<?xml version="1.0" encoding="UTF-8"?>
<MedicineInformation>
	<Header>
		<Title>GuildLink image listing for December 2022</Title>
		<Timestamp>02/12/2022 15:31</Timestamp>
		<schemaversion>2.5</schemaversion>
		<sequence>174</sequence>
        <presentationcount>4635</presentationcount>
		<disclaimers>
			<medicationdisclaimer id="1">*Actual image may differ</medicationdisclaimer>
			<reportdisclaimer id="1">*The appearance of your medication may have changed. Please check with your pharmacist</reportdisclaimer>
		</disclaimers>
	</Header>
	<Brands>
<Brand>
			<brandname>3TC</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>54313</Austr>
				<PresentationName>3TC Tablets</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Lamivudine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>3TC Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>vic3tctb11121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lamivudine</ActiveIngredient>
						<ReleaseDate>2021-11-11 16:41:47.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 13:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>diamond-shaped</Shape>
							<Side1Marking>GX CJ7</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>54313-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>81359</Austr>
				<PresentationName>3TC Tablets</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Lamivudine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>3TC Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>vic3tctb11121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lamivudine</ActiveIngredient>
						<ReleaseDate>2021-11-11 16:41:47.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 13:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>grey</Colour>
							<Scoring>unscored</Scoring>
							<Shape>diamond-shaped</Shape>
							<Side1Marking>GX EJ7</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>81359-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Abacavir/lamivudine (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>239753</Austr>
				<PresentationName>Abacavir/lamivudine 600/300 APOTEX</PresentationName>
    			<PresentionStrength>600mg/300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Abacavir sulfate,Lamivudine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/09/2018 09:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified capsule-shaped</Shape>
							<Side1Marking>600/300</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>239753-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Abacavir/lamivudine (Viatris)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>266516</Austr>
				<PresentationName>Abacavir/lamivudine Viatris</PresentationName>
    			<PresentionStrength>600mg/300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Abacavir sulfate,Lamivudine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abacavir/Lamivudine Viatris</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcablam10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>abacavir sulfate with lamivudine</ActiveIngredient>
						<ReleaseDate>2022-08-02 13:03:32.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/12/2018 14:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified capsule-shaped</Shape>
							<Side1Marking>AL 12</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>266516-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Abilify</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>90925</Austr>
				<PresentationName>Abilify</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abilify</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oscabili11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>aripiprazole</ActiveIngredient>
						<ReleaseDate>2022-10-31 14:31:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2015 15:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rectangular-shaped</Shape>
							<Side1Marking>A-007 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>90925-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>90997</Austr>
				<PresentationName>Abilify</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abilify</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oscabili11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>aripiprazole</ActiveIngredient>
						<ReleaseDate>2022-10-31 14:31:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2015 15:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rectangular-shaped</Shape>
							<Side1Marking>A-008 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>90997-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>90998</Austr>
				<PresentationName>Abilify</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abilify</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oscabili11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>aripiprazole</ActiveIngredient>
						<ReleaseDate>2022-10-31 14:31:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2015 15:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>A-009 15</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>90998-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>90999</Austr>
				<PresentationName>Abilify</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abilify</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oscabili11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>aripiprazole</ActiveIngredient>
						<ReleaseDate>2022-10-31 14:31:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2015 15:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to pale yellowish white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>A-010 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>90999-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>91000</Austr>
				<PresentationName>Abilify</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abilify</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oscabili11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>aripiprazole</ActiveIngredient>
						<ReleaseDate>2022-10-31 14:31:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2015 15:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>A-011 30</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>91000-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Abisart</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>302142</Austr>
				<PresentationName>Abisart</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abisart</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcabisa10819</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>irbesartan</ActiveIngredient>
						<ReleaseDate>2019-08-15 08:20:24.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/10/2020 13:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>I3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>302142-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>302143</Austr>
				<PresentationName>Abisart</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abisart</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcabisa10819</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>irbesartan</ActiveIngredient>
						<ReleaseDate>2019-08-15 08:20:24.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/10/2020 13:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>I4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>302143-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>302144</Austr>
				<PresentationName>Abisart</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abisart</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcabisa10819</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>irbesartan</ActiveIngredient>
						<ReleaseDate>2019-08-15 08:20:24.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/02/2020 12:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>I5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>302144-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Abisart HCTZ</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>302148</Austr>
				<PresentationName>Abisart HCTZ</PresentationName>
    			<PresentionStrength>300/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abisart HCTZ</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcabisz10819</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>irbesartan with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2019-08-15 08:20:14.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/02/2020 12:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>IH3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>302148-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>302149</Austr>
				<PresentationName>Abisart HCTZ</PresentationName>
    			<PresentionStrength>300mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abisart HCTZ</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcabisz10819</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>irbesartan with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2019-08-15 08:20:14.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/06/2019 06:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink to red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>IH 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>302149-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Abstral</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>193332</Austr>
				<PresentationName>Abstral</PresentationName>
    			<PresentionStrength>100mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fentanyl citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abstral sublingual tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fkcabsst10820</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fentanyl citrate</ActiveIngredient>
						<ReleaseDate>2020-08-04 13:19:47.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/09/2018 08:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>193332-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>193335</Austr>
				<PresentationName>Abstral</PresentationName>
    			<PresentionStrength>200mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fentanyl citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abstral sublingual tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fkcabsst10820</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fentanyl citrate</ActiveIngredient>
						<ReleaseDate>2020-08-04 13:19:47.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/09/2018 08:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>193335-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>193336</Austr>
				<PresentationName>Abstral</PresentationName>
    			<PresentionStrength>400mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fentanyl citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abstral sublingual tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fkcabsst10820</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fentanyl citrate</ActiveIngredient>
						<ReleaseDate>2020-08-04 13:19:47.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/09/2018 08:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>diamond-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>193336-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>228199</Austr>
				<PresentationName>Abstral</PresentationName>
    			<PresentionStrength>300mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fentanyl citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abstral sublingual tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fkcabsst10820</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fentanyl citrate</ActiveIngredient>
						<ReleaseDate>2020-08-04 13:19:47.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/09/2018 08:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>arc triangle-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>228199-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>228208</Austr>
				<PresentationName>Abstral</PresentationName>
    			<PresentionStrength>600mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fentanyl citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abstral sublingual tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fkcabsst10820</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fentanyl citrate</ActiveIngredient>
						<ReleaseDate>2020-08-04 13:19:47.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/09/2018 08:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>D-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>228208-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>228209</Austr>
				<PresentationName>Abstral</PresentationName>
    			<PresentionStrength>800mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fentanyl citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abstral sublingual tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fkcabsst10820</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fentanyl citrate</ActiveIngredient>
						<ReleaseDate>2020-08-04 13:19:47.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/09/2018 08:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>caplet-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>228209-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Abyraz</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>159503</Austr>
				<PresentationName>Abyraz</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abyraz</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcabyra10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>aripiprazole</ActiveIngredient>
						<ReleaseDate>2022-07-19 11:20:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/11/2018 17:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>ARZ 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159503-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>159504</Austr>
				<PresentationName>Abyraz</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abyraz</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcabyra10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>aripiprazole</ActiveIngredient>
						<ReleaseDate>2022-07-19 11:20:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/11/2018 17:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ARZ 30</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159504-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>159505</Austr>
				<PresentationName>Abyraz</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abyraz</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcabyra10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>aripiprazole</ActiveIngredient>
						<ReleaseDate>2022-07-19 11:20:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/11/2018 17:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ARZ 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159505-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>159506</Austr>
				<PresentationName>Abyraz</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Abyraz</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcabyra10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>aripiprazole</ActiveIngredient>
						<ReleaseDate>2022-07-19 11:20:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/11/2018 17:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ARZ 15</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159506-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Acamprosate (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>286652</Austr>
				<PresentationName>APO-Acamprosate</PresentationName>
    			<PresentionStrength>333mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>25/09/2018 09:18</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>300</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>286652-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Acamprosate calcium (Mylan)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>298641</Austr>
				<PresentationName>Acamprosate Mylan</PresentationName>
    			<PresentionStrength>333mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Acamprosate calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Acamprosate Mylan </DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>acamprosate calcium</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>02/05/2019 08:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>333</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>298641-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Acarbose (Viatris)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>226796</Austr>
				<PresentationName>Acarbose Viatris</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Acarbose</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Acarbose Viatris</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>acarbose</ActiveIngredient>
						<ReleaseDate>2022-03-14 07:50:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>28/11/2018 17:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ACA 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>226796-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>226797</Austr>
				<PresentationName>Acarbose Viatris</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Acarbose</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Acarbose Viatris</DocumentName>
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							<AvailableFormats>
								<Format>PDF</Format>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ACA 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>226797-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Accupril</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>40926</Austr>
				<PresentationName>Accupril</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quinapril hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Accupril</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>quinapril hydrochloride</ActiveIngredient>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/08/2008 09:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish-brown</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking>5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>40926-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>40928</Austr>
				<PresentationName>Accupril</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quinapril hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Accupril</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>quinapril hydrochloride</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/08/2008 09:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish-brown</Colour>
							<Scoring>scored</Scoring>
							<Shape>triangular</Shape>
							<Side1Marking>1 0</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>40928-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>40930</Austr>
				<PresentationName>Accupril</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quinapril hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Accupril</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcaccut10922</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>quinapril hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-09-02 09:59:51.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/08/2008 09:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish-brown</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>2 0</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>40930-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Accuretic</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>81930</Austr>
				<PresentationName>Accuretic</PresentationName>
    			<PresentionStrength>10mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Quinapril hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Accuretic</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcacret10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>quinapril hydrochloride with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2022-07-27 10:16:29.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/09/2011 15:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>81930-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>81931</Austr>
				<PresentationName>Accuretic</PresentationName>
    			<PresentionStrength>20mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quinapril hydrochloride,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Accuretic</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcacret10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>quinapril hydrochloride with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2022-07-27 10:16:29.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/08/2008 09:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>triangular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>81931-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Acetec</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>75497</Austr>
				<PresentationName>Acetec</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Enalapril maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Acetec</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>enalapril maleate</ActiveIngredient>
						<ReleaseDate>2019-11-07 09:55:38.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/07/2011 13:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>arc triangle</Shape>
							<Side1Marking>5 G</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75497-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>75498</Austr>
				<PresentationName>Acetec</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Enalapril maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Acetec</DocumentName>
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							<AvailableFormats>
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						</DocumentTypes>
						<ActiveIngredient>enalapril maleate</ActiveIngredient>
						<ReleaseDate>2019-11-07 09:55:38.0</ReleaseDate>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>rusty red</Colour>
							<Scoring>scored</Scoring>
							<Shape>arc triangle</Shape>
							<Side1Marking>10 G</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75498-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>75499</Austr>
				<PresentationName>Acetec</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Enalapril maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Acetec</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
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						<ActiveIngredient>enalapril maleate</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>scored</Scoring>
							<Shape>arc triangle</Shape>
							<Side1Marking>20 G</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75499-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aciclovir (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>159140</Austr>
				<PresentationName>APO-Aciclovir </PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-07-27 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Aciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/09/2018 12:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>APO 200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159140-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>159141</Austr>
				<PresentationName>APO-Aciclovir </PresentationName>
    			<PresentionStrength>800mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Aciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/09/2018 12:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>APO 800</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159141-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>182881</Austr>
				<PresentationName>Aciclovir Apotex</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>aciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/08/2021 16:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>ACV</Side1Marking>
							<Side2Marking>200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>182881-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>182883</Austr>
				<PresentationName>Aciclovir Apotex</PresentationName>
    			<PresentionStrength>800mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>aciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/08/2021 16:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>ACV</Side1Marking>
							<Side2Marking>800</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>182883-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aciclovir (Generic Health)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>183860</Austr>
				<PresentationName>Aciclovir GH</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>ACV</Side1Marking>
							<Side2Marking>200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183860-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aciclovir (GenRx)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>71816</Austr>
				<PresentationName>GenRx Aciclovir</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Aciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/08/2008 14:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>APO 200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>71816-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>71817</Austr>
				<PresentationName>GenRx Aciclovir</PresentationName>
    			<PresentionStrength>800mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Aciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/08/2008 14:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>APO 800</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>71817-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aciclovir (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>130607</Austr>
				<PresentationName>Aciclovir</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/09/2009 15:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>APO 200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>130607-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>130608</Austr>
				<PresentationName>Aciclovir</PresentationName>
    			<PresentionStrength>800mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/09/2009 15:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>APO 800</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>130608-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aciclovir (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>99420</Austr>
				<PresentationName>Aciclovir Sandoz</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Aciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>99420-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>99421</Austr>
				<PresentationName>Aciclovir Sandoz</PresentationName>
    			<PresentionStrength>800mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Aciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>99421-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Acimax</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>67306</Austr>
				<PresentationName>Acimax</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Omeprazole magnesium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>20mg</Side1Marking>
							<Side2Marking>logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>67306-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Acquin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>192146</Austr>
				<PresentationName>Acquin</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 12:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192146-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>192147</Austr>
				<PresentationName>Acquin</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 12:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192147-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>192148</Austr>
				<PresentationName>Acquin</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 12:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192148-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Actaze</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>254272</Austr>
				<PresentationName>Actaze</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 12:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PIO</Side1Marking>
							<Side2Marking>15</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>254272-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>254292</Austr>
				<PresentationName>Actaze</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 12:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PIO</Side1Marking>
							<Side2Marking>30</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>254292-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>254312</Austr>
				<PresentationName>Actaze</PresentationName>
    			<PresentionStrength>45mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 12:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PIO</Side1Marking>
							<Side2Marking>45</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>254312-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Actiq</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>91598</Austr>
				<PresentationName>Actiq</PresentationName>
    			<PresentionStrength>200mcg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fentanyl citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Actiq</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcactiq10821</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fentanyl citrate</ActiveIngredient>
						<ReleaseDate>2021-08-12 16:52:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/06/2009 14:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Lozenges</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>cylindrical</Shape>
							<Side1Marking>ACTIQ 200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>91598-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>91600</Austr>
				<PresentationName>Actiq</PresentationName>
    			<PresentionStrength>400mcg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fentanyl citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Actiq</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcactiq10821</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fentanyl citrate</ActiveIngredient>
						<ReleaseDate>2021-08-12 16:52:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Lozenges</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape></Shape>
							<Side1Marking>ACTIQ 400</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>91600-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>91601</Austr>
				<PresentationName>Actiq</PresentationName>
    			<PresentionStrength>600mcg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fentanyl citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Actiq</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcactiq10821</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fentanyl citrate</ActiveIngredient>
						<ReleaseDate>2021-08-12 16:52:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Lozenges</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape></Shape>
							<Side1Marking>ACTIQ 600</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>91601-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>91602</Austr>
				<PresentationName>Actiq</PresentationName>
    			<PresentionStrength>800mcg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fentanyl citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Actiq</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcactiq10821</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fentanyl citrate</ActiveIngredient>
						<ReleaseDate>2021-08-12 16:52:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Lozenges</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape></Shape>
							<Side1Marking>ACTIQ 800</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>91602-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Actonel</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>117667</Austr>
				<PresentationName>Actonel Combi</PresentationName>
    			<PresentionStrength>35mg+1250mg</PresentionStrength>
    			<PresentationForm>Combination Pack</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Calcium carbonate,Risedronate sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>35mg</Side1Marking>
							<Side2Marking>RSN</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>117667-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>NE2</Side1Marking>
							<Side2Marking>NE2</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>117667-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>150618</Austr>
				<PresentationName>Actonel</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risedronate sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Actonel</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ttcacton30421</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>risedronate sodium</ActiveIngredient>
						<ReleaseDate>2021-04-29 10:08:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/07/2011 14:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>150mg</Side1Marking>
							<Side2Marking>RSN</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>150618-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166838</Austr>
				<PresentationName>Actonel EC</PresentationName>
    			<PresentionStrength>35mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risedronate sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Actonel EC</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ttcactec10421</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>risedronate sodium</ActiveIngredient>
						<ReleaseDate>2021-04-20 13:29:33.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/07/2011 14:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>EC 35</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166838-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166853</Austr>
				<PresentationName>Actonel EC Combi</PresentationName>
    			<PresentionStrength>35mg+1250mg</PresentionStrength>
    			<PresentationForm>Combination Pack</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risedronate sodium,Calcium carbonate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/09/2011 13:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Combination Pack</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>EC 35</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166853-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Combination Pack</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>NE2</Side1Marking>
							<Side2Marking>NE2</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166853-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>74135</Austr>
				<PresentationName>Actonel</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risedronate sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Actonel</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ttcacton30421</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>risedronate sodium</ActiveIngredient>
						<ReleaseDate>2021-04-29 10:08:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/09/2011 13:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>5mg</Side1Marking>
							<Side2Marking>RSN</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>74135-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>74136</Austr>
				<PresentationName>Actonel</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risedronate sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Actonel</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ttcacton30421</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>risedronate sodium</ActiveIngredient>
						<ReleaseDate>2021-04-29 10:08:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/07/2011 14:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>30mg</Side1Marking>
							<Side2Marking>RSN</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>74136-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>82746</Austr>
				<PresentationName>Actonel</PresentationName>
    			<PresentionStrength>35mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risedronate sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>35mg</Side1Marking>
							<Side2Marking>RSN</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82746-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Actos</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>76462</Austr>
				<PresentationName>Actos</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pioglitazone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/02/2009 09:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ACTOS</Side1Marking>
							<Side2Marking>15</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>76462-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>76463</Austr>
				<PresentationName>Actos</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pioglitazone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/02/2009 09:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ACTOS</Side1Marking>
							<Side2Marking>30</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>76463-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>76464</Austr>
				<PresentationName>Actos</PresentationName>
    			<PresentionStrength>45mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pioglitazone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/02/2009 09:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ACTOS</Side1Marking>
							<Side2Marking>45</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>76464-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Adalat</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>18691</Austr>
				<PresentationName>Adalat</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/04/2010 10:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink-grey</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>1 U</Side1Marking>
							<Side2Marking>BAYER Cross</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>18691-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>43103</Austr>
				<PresentationName>Adalat</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/04/2010 10:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink-grey</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>A 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>43103-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>60101</Austr>
				<PresentationName>Adalat Oros</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/04/2010 10:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>rose pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Adalat 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>60101-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>76040</Austr>
				<PresentationName>Adalat Oros</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/04/2010 10:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>rose pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>60</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>76040-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>76041</Austr>
				<PresentationName>Adalat Oros</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/04/2010 10:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>rose pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>30</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>76041-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Adcirca</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>172882</Austr>
				<PresentationName>Adcirca</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Tadalafil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Adcirca</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>lycadcir10221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tadalafil</ActiveIngredient>
						<ReleaseDate>2021-03-02 14:11:36.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/10/2011 10:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>almond-shaped</Shape>
							<Side1Marking>4467</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>172882-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Addos XR</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>114825</Austr>
				<PresentationName>Addos XR</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/04/2012 14:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>30</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>114825-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>98806</Austr>
				<PresentationName>Addos XR</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 12:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>60</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>98806-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Adefin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>91778</Austr>
				<PresentationName>Adefin XL</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nifedipine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Adefin XL</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>nifedipine</ActiveIngredient>
						<ReleaseDate>2020-01-15 07:09:25.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>60</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>91778-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>91779</Austr>
				<PresentationName>Adefin XL</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nifedipine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Adefin XL</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>nifedipine</ActiveIngredient>
						<ReleaseDate>2020-01-15 07:09:25.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>30</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>91779-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>92999</Austr>
				<PresentationName>Adefin</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nifedipine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Adefin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>nifedipine</ActiveIngredient>
						<ReleaseDate>2020-01-15 07:09:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink-grey</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>A 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>92999-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>93000</Austr>
				<PresentationName>Adefin</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nifedipine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Adefin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>nifedipine</ActiveIngredient>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink-grey</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>1 U</Side1Marking>
							<Side2Marking>BAYER cross</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>93000-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Adefovir dipivoxil (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>212048</Austr>
				<PresentationName>APO-Adefovir </PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Adefovir dipivoxil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>06/01/2016 14:33</DateEffective>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>A10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>212048-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Adenuric</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>205556</Austr>
				<PresentationName>Adenuric</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>febuxostat</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Adenuric tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fkcadent11122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>febuxostat</ActiveIngredient>
						<ReleaseDate>2022-11-07 16:45:49.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/09/2018 08:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow to yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>rectangular-shaped</Shape>
							<Side1Marking>80</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>205556-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Adesan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>171016</Austr>
				<PresentationName>Adesan</PresentationName>
    			<PresentionStrength>16mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Adesan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>candesartan cilexetil</ActiveIngredient>
						<ReleaseDate>2019-12-12 13:36:13.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>mottled pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>31</Side1Marking>
							<Side2Marking>MC</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>171016-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>171017</Austr>
				<PresentationName>Adesan</PresentationName>
    			<PresentionStrength>32mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Adesan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcadesa11219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>candesartan cilexetil</ActiveIngredient>
						<ReleaseDate>2019-12-12 13:36:13.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>mottled pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>MC 32</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>171017-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>171019</Austr>
				<PresentationName>Adesan</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Adesan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcadesa11219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>candesartan cilexetil</ActiveIngredient>
						<ReleaseDate>2019-12-12 13:36:13.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>24</Side1Marking>
							<Side2Marking>MC</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>171019-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>171022</Austr>
				<PresentationName>Adesan</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Adesan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcadesa11219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>candesartan cilexetil</ActiveIngredient>
						<ReleaseDate>2019-12-12 13:36:13.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>mottled pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>25</Side1Marking>
							<Side2Marking>MC</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>171022-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Adesan HCT</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>163670</Austr>
				<PresentationName>Adesan HCT</PresentationName>
    			<PresentionStrength>16mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Candesartan cilexetil,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Adesan HCT</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcadehc10719</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>candesartan cilexetil with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2019-08-05 09:17:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CH2</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>163670-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>206485</Austr>
				<PresentationName>Adesan HCT</PresentationName>
    			<PresentionStrength>32mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Candesartan cilexetil,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Adesan HCT</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcadehc10719</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>candesartan cilexetil with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2019-08-05 09:17:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/10/2016 14:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow mottled</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CH 3</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>206485-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>206486</Austr>
				<PresentationName>Adesan HCT</PresentationName>
    			<PresentionStrength>32mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Adesan HCT</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>candesartan cilexetil with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2019-08-05 09:17:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/03/2018 12:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach mottled</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CH 4</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>206486-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Advagraf XL</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>269212</Austr>
				<PresentationName>Advagraf XL</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tacrolimus</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Prograf and Advagraf XL</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tacrolimus</ActiveIngredient>
						<ReleaseDate>2022-11-14 16:06:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/08/2016 15:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light yellow and orange</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>0.5mg</Side1Marking>
							<Side2Marking>(Logo) 647</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>269212-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>269214</Austr>
				<PresentationName>Advagraf XL</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tacrolimus</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Prograf and Advagraf XL</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>axcprogr11122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tacrolimus</ActiveIngredient>
						<ReleaseDate>2022-11-14 16:06:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/08/2016 15:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and orange</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>1mg</Side1Marking>
							<Side2Marking>(Logo) 677</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>269214-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>269215</Austr>
				<PresentationName>Advagraf XL</PresentationName>
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			<Presentations>
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			<Presentations>
				<Austr>70852</Austr>
				<PresentationName>Akamin</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>minocycline hydrochloride dihydrate</TGAIngredient>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Side1Marking>MC</Side1Marking>
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			<brandname>Akynzeo</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>222237</Austr>
				<PresentationName>Akynzeo</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Palonosetron hydrochloride,netupitant</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
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			<brandname>Aldactone</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>68953</Austr>
				<PresentationName>Aldactone</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>buff</Colour>
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							<Side1Marking>SEARLE 39</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>68954</Austr>
				<PresentationName>Aldactone</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Spironolactone</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcaldat10722</Filename>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Side1Marking>SEARLE 134</Side1Marking>
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		</Brand><Brand>
			<brandname>Aldomet</brandname>
			<isamtbrand>true</isamtbrand>
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				<PresentationName>Aldomet</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient>Methyldopa</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>123863</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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		</Brand><Brand>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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    			<PresentionStrength>70mg/140mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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						<DateEffective>26/08/2019 21:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified capsule-shaped</Shape>
							<Side1Marking>ADC</Side1Marking>
							<Side2Marking>56</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>308733-C01-01-BL600.jpg</ImageFileName>
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		</Brand><Brand>
			<brandname>Alendronate Plus D3 and Calcium (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>222684</Austr>
				<PresentationName>Alendronate Plus D3 and Calcium</PresentationName>
    			<PresentionStrength>70mg/140mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>composite pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/07/2016 11:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified capsule shaped</Shape>
							<Side1Marking>ADC</Side1Marking>
							<Side2Marking>56</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>222684-C01-01-BL600.jpg</ImageFileName>
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							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark green</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>222684-C02-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Alepam</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>17572</Austr>
				<PresentationName>Alepam</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Oxazepam</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Alepam</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcalepa10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>oxazepam</ActiveIngredient>
						<ReleaseDate>2022-05-20 18:30:31.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>OM 15</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>17572-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>17573</Austr>
				<PresentationName>Alepam</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Oxazepam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Alepam</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcalepa10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>oxazepam</ActiveIngredient>
						<ReleaseDate>2022-05-20 18:30:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>OM 30</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>17573-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Alka-Seltzer</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>15683</Austr>
				<PresentationName>Alka-Seltzer Original</PresentationName>
    			<PresentionStrength>324mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2009 15:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ALKA SELTZER</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>15683-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>15683-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>15684</Austr>
				<PresentationName>Alka-Seltzer Lemon</PresentationName>
    			<PresentionStrength>324mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2009 15:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ALKA SELTZER</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>15684-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>15684-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Alkeran</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>81543</Austr>
				<PresentationName>Alkeran Tablets</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Melphalan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/10/2010 08:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>GX EH3</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>81543-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Allegron</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>14619</Austr>
				<PresentationName>Allegron</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nortriptyline</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/11/2008 13:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>14619-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>53747</Austr>
				<PresentationName>Allegron</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nortriptyline</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/11/2008 13:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>53747-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Allereze</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>117492</Austr>
				<PresentationName>Allereze</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>loratadine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Allereze</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>loratadine</ActiveIngredient>
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				<Images>
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						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>LR 10</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>117492-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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		</Brand><Brand>
			<brandname>Allersoothe</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>160733</Austr>
				<PresentationName>Allersoothe</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<DateEffective>03/09/2010 14:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>160733-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>160734</Austr>
				<PresentationName>Allersoothe</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>160734-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Allopurinol (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>218874</Austr>
				<PresentationName>APO-Allopurinol</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
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							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>U4A</Side1Marking>
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							<Views>
							<View>
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						</Phase>
					</Versions>
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			</Presentations>
			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-07-27 00:00:00'}</WithdrawalDate>
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							<Scoring>scored</Scoring>
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							<Side1Marking>C9B</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>218875-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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			</Presentations>
			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
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							<Colour>peach</Colour>
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							<Side1Marking>AL 300</Side1Marking>
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			<Presentations>
				<Austr>269652</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Allopurinol</TGAIngredient>
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						<VersionSequence>1</VersionSequence>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AL 100</Side1Marking>
							<Side2Marking></Side2Marking>
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							<View>
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								<ImageFileName>269652-C01-01-BL600.jpg</ImageFileName>
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		</Brand><Brand>
			<brandname>Allopurinol (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>219912</Austr>
				<PresentationName>Chemmart Allopurinol </PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>U4A</Side1Marking>
							<Side2Marking></Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>219912-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>219913</Austr>
				<PresentationName>Chemmart Allopurinol</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C9B</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>219913-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Allopurinol (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>65905</Austr>
				<PresentationName>Allopurinol Sandoz</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Allopurinol</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>65905-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>65906</Austr>
				<PresentationName>Allopurinol Sandoz</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Allopurinol</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>25/09/2008 16:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>65906-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
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			</Presentations>
		</Brand><Brand>
			<brandname>Allopurinol (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>219904</Austr>
				<PresentationName>Terry White Chemists Allopurinol </PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<VersionSequence>1</VersionSequence>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>U4A</Side1Marking>
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							<Views>
							<View>
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			<Presentations>
				<Austr>219905</Austr>
				<PresentationName>Terry White Chemists Allopurinol </PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C9B</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>83101</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Allopurinol</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Shape>round</Shape>
							<Side1Marking>ALL 100</Side1Marking>
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			<Presentations>
				<Austr>83102</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Allopurinol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
							<Side1Marking>ALL 300</Side1Marking>
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							<Views>
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			<brandname>Allosig</brandname>
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			<Presentations>
				<Austr>286084</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
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							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
							<Side1Marking>AP 100</Side1Marking>
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			<Presentations>
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				<PresentationName>Allosig</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Views>
							<View>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>54009</Austr>
				<PresentationName>Alodorm</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
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    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DocumentName>Alodorm</DocumentName>
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							<Views>
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							<View>
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			<brandname>Alphaclav</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>230395</Austr>
				<PresentationName>Alphaclav</PresentationName>
    			<PresentionStrength>500/125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amoxycillin trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Alphamox</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcaamox10122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amoxicillin trihydrate</ActiveIngredient>
						<ReleaseDate>2022-01-11 15:12:06.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green and cream</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>17678-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>17679</Austr>
				<PresentationName>Alphamox</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amoxycillin trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Alphamox</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcaamox10122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amoxicillin trihydrate</ActiveIngredient>
						<ReleaseDate>2022-01-11 15:12:06.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green and cream</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>17679-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Alphapress</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>17575</Austr>
				<PresentationName>Alphapress</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Hydralazine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Alphapress</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcapres20919</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>hydralazine hydrochloride</ActiveIngredient>
						<ReleaseDate>2019-09-27 14:20:18.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>cream</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>17575-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>60380</Austr>
				<PresentationName>Alphapress</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Hydralazine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Alphapress</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcapres20919</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>hydralazine hydrochloride</ActiveIngredient>
						<ReleaseDate>2019-09-27 14:20:18.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>HE 50</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>60380-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Alprax</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>82638</Austr>
				<PresentationName>Alprax</PresentationName>
    			<PresentionStrength>0.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>A 25</Side1Marking>
							<Side2Marking>Arrow logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82638-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>82640</Austr>
				<PresentationName>Alprax</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>A 5</Side1Marking>
							<Side2Marking>Arrow logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82640-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>82643</Austr>
				<PresentationName>Alprax</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>A 1</Side1Marking>
							<Side2Marking>Arrow logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82643-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>82644</Austr>
				<PresentationName>Alprax</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>rectangular-shaped</Shape>
							<Side1Marking>A 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82644-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Alprazolam (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>82798</Austr>
				<PresentationName>Alprazolam-GA</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/09/2009 09:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>APO 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82798-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>82799</Austr>
				<PresentationName>Alprazolam-GA</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 11:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>rectangular-shaped</Shape>
							<Side1Marking>APO 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82799-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Alprazolam (GenRx)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>79802</Austr>
				<PresentationName>GenRx Alprazolam</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Alprazolam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/08/2008 14:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>APO 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>79802-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>80934</Austr>
				<PresentationName>GenRx Alprazolam</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Alprazolam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/08/2008 14:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>rectangular-shaped</Shape>
							<Side1Marking>APO 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>80934-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Alprim</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>63518</Austr>
				<PresentationName>Alprim</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Trimethoprim</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Alprim</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>trimethoprim</ActiveIngredient>
						<ReleaseDate>2022-05-11 16:05:50.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TM 300</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>63518-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Alu-Tab</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>58664</Austr>
				<PresentationName>Alu-Tab</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/04/2009 12:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>3M</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>58664-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Alzene</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>116582</Austr>
				<PresentationName>Alzene</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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   				<WithdrawalDate></WithdrawalDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 14:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>140231-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amira (Mylan)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>288711</Austr>
				<PresentationName>Amira</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Moclobemide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Amira 150 and Amira 300</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>moclobemide</ActiveIngredient>
						<ReleaseDate>2022-03-21 09:37:00.0</ReleaseDate>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2019 14:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>288711-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>288712</Austr>
				<PresentationName>Amira</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Moclobemide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Amira 150 and Amira 300</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>moclobemide</ActiveIngredient>
						<ReleaseDate>2022-03-21 09:37:00.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/12/2018 14:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to yellow-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>288712-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amisulpride (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>178898</Austr>
				<PresentationName>APO-Amisulpride</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amisulpride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/05/2012 10:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>178898-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>178902</Austr>
				<PresentationName>APO-Amisulpride</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amisulpride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/05/2012 11:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>178902-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>178904</Austr>
				<PresentationName>APO-Amisulpride</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amisulpride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/05/2012 11:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>178904-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amisulpride (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>128985</Austr>
				<PresentationName>Amisulpride Sandoz</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amisulpride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AMI 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>128985-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>128993</Austr>
				<PresentationName>Amisulpride Sandoz</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amisulpride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AMI 200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>128993-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>128993-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>128994</Austr>
				<PresentationName>Amisulpride Sandoz</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amisulpride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>AMI 400</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>128994-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amisulpride (Winthrop)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>125165</Austr>
				<PresentationName>Amisulpride Winthrop</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amisulpride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Amisulpride Winthrop</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcamisu10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amisulpride</ActiveIngredient>
						<ReleaseDate>2022-09-26 18:21:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/09/2008 09:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>AMI 400</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>125165-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>125173</Austr>
				<PresentationName>Amisulpride Winthrop</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amisulpride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Amisulpride Winthrop</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcamisu10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amisulpride</ActiveIngredient>
						<ReleaseDate>2022-09-26 18:21:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AMI 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>125173-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>125174</Austr>
				<PresentationName>Amisulpride Winthrop</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amisulpride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Amisulpride Winthrop</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amisulpride</ActiveIngredient>
						<ReleaseDate>2022-09-26 18:21:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AMI 200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>125174-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>125174-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>amitriptyline hydrochloride (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>215351</Austr>
				<PresentationName>APO-Amitriptyline </PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amitriptyline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>IA 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>215351-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>215367</Austr>
				<PresentationName>APO-Amitriptyline </PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amitriptyline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>IA 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>215367-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>215380</Austr>
				<PresentationName>APO-Amitriptyline </PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amitriptyline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>215380-C01-01-BL600.jpg</ImageFileName>
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			<brandname>Amitriptyline Hydrochloride (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
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    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
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								<ViewLabel>C</ViewLabel>
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			<Presentations>
				<Austr>215403</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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							<Side2Marking></Side2Marking>
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								<ImageFileName>215403-C01-01-BL600.jpg</ImageFileName>
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			<brandname>Amitriptyline Hydrochloride (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
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				<Austr>215356</Austr>
				<PresentationName>Terry White Chemists Amitriptyline</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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							<Colour>yellow</Colour>
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								<ViewLabel>C</ViewLabel>
								<ImageFileName>215356-C01-01-BL600.jpg</ImageFileName>
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			<Presentations>
				<Austr>215358</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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							<Shape>circular</Shape>
							<Side1Marking>IA 10</Side1Marking>
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								<ImageFileName>215358-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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			<Presentations>
				<Austr>215364</Austr>
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    			<PresentionStrength>50mg</PresentionStrength>
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								<ViewLabel>C</ViewLabel>
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			<Presentations>
				<Austr>232796</Austr>
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							<Colour>blue</Colour>
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			<Presentations>
				<Austr>232797</Austr>
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    			<PresentionStrength>25mg</PresentionStrength>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amitriptyline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
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			<Presentations>
				<Austr>201371</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate>{ts '2022-07-27 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/07/2011 10:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AML 10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135125-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>135145</Austr>
				<PresentationName>Apo-Amlodipine</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/07/2011 10:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AML 5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135145-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>135146</Austr>
				<PresentationName>Apo-Amlodipine</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/07/2011 10:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AML 10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135146-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>307471</Austr>
				<PresentationName>Amlodipine Apotex</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/08/2019 21:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>E21</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>307471-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>307472</Austr>
				<PresentationName>Amlodipine Apotex</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/08/2019 21:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>307472-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amlodipine (Blooms the Chemist)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>135127</Austr>
				<PresentationName>Blooms the Chemist Amlodipine </PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 21:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AML 5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135127-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>135128</Austr>
				<PresentationName>Blooms the Chemist Amlodipine </PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>amlodipine besilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 21:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AML 10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135128-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amlodipine (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>135130</Austr>
				<PresentationName>Chemmart Amlodipine</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/08/2008 09:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AML 5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135130-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>135131</Austr>
				<PresentationName>Chemmart Amlodipine</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/08/2008 09:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AML 10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135131-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amlodipine (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>139275</Austr>
				<PresentationName>Amlodipine-GA</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 11:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>elongated octagonal</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>139275-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>139303</Austr>
				<PresentationName>Amlodipine-GA</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 11:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>octagonal</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>139303-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amlodipine (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>140104</Austr>
				<PresentationName>Amlodipine GH</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/04/2012 23:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>octagon-shaped</Shape>
							<Side1Marking>AM 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>140104-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>140140</Austr>
				<PresentationName>Amlodipine GH</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/09/2011 15:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>octagon-shaped</Shape>
							<Side1Marking>AM 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>140140-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amlodipine (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>215706</Austr>
				<PresentationName>Pharmacor Amlodipine</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/01/2016 10:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>octagonal</Shape>
							<Side1Marking>209 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>215706-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>215709</Austr>
				<PresentationName>Pharmacor Amlodipine</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/01/2016 10:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>octagonal</Shape>
							<Side1Marking>210 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>215709-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amlodipine (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>124578</Austr>
				<PresentationName>Amlodipine Sandoz</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/09/2008 16:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to almost white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>124578-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>124582</Austr>
				<PresentationName>Amlodipine Sandoz</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/09/2008 16:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to almost white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>124582-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amlodipine (Spirit)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>96950</Austr>
				<PresentationName>Amlodipine Spirit</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2011 13:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96950-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>96962</Austr>
				<PresentationName>Amlopipine Spirit</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2011 12:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>10 MH</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96962-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amlodipine (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>135135</Austr>
				<PresentationName>Terry White Chemists Amlodipine</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/08/2008 09:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AML 5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135135-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>135136</Austr>
				<PresentationName>Terry White Chemists Amlodipine</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/08/2008 09:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AML 10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135136-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amlodipine/Atorvastatin (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>214345</Austr>
				<PresentationName>APO-Amlodipine/Atorvastatin</PresentationName>
    			<PresentionStrength>10mg/40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-07-27 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besylate,Atorvastatin calcium propylene glycol solvate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>10/40</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214345-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>214359</Austr>
				<PresentationName>APO-Amlodipine/Atorvastatin</PresentationName>
    			<PresentionStrength>10mg/80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-07-27 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besylate,Atorvastatin calcium propylene glycol solvate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>10/80</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214359-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>214360</Austr>
				<PresentationName>APO-Amlodipine/Atorvastatin</PresentationName>
    			<PresentionStrength>10mg/20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-07-27 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium propylene glycol solvate,Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>10/20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214360-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>214375</Austr>
				<PresentationName>APO-Amlodipine/Atorvastatin</PresentationName>
    			<PresentionStrength>5mg/40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-07-27 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besylate,Atorvastatin calcium propylene glycol solvate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>5/40</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214375-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>214378</Austr>
				<PresentationName>APO-Amlodipine/Atorvastatin</PresentationName>
    			<PresentionStrength>5mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-07-27 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besylate,Atorvastatin calcium propylene glycol solvate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>5/10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214378-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>214385</Austr>
				<PresentationName>APO-Amlodipine/Atorvastatin</PresentationName>
    			<PresentionStrength>5mg/20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-07-27 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium propylene glycol solvate,Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>5/20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214385-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>214386</Austr>
				<PresentationName>APO-Amlodipine/Atorvastatin</PresentationName>
    			<PresentionStrength>5mg/80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-07-27 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besylate,Atorvastatin calcium propylene glycol solvate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>5/80</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214386-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>214409</Austr>
				<PresentationName>APO-Amlodipine/Atorvastatin</PresentationName>
    			<PresentionStrength>10mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-07-27 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besylate,Atorvastatin calcium propylene glycol solvate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>10/10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214409-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amlodipine/Valsartan (Novartis)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>151626</Austr>
				<PresentationName>Amlodipine/Valsartan Novartis</PresentationName>
    			<PresentionStrength>80mg/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan,Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Amlodipine/Valsartan Novartis</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcvaaor20620</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amlodipine besilate with valsartan</ActiveIngredient>
						<ReleaseDate>2020-07-20 11:08:58.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/02/2013 13:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NV</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151626-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amlodipine/Valsartan/HCT (Novartis)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>158161</Austr>
				<PresentationName>Amlodipine/Valsartan/HCT Novartis</PresentationName>
    			<PresentionStrength>5mg/160mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Amlodipine besylate,Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Amlodipine/Valsartan/HCT Novartis</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcvahor11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amlodipine besilate with valsartan and hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2022-11-02 16:42:04.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/02/2013 13:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>ovaloid</Shape>
							<Side1Marking>VCL</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158161-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amoxil</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>11131</Austr>
				<PresentationName>Amoxil</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-08 00:00:00'}</WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Amoxycillin trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 13:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>AMOXIL</Side1Marking>
							<Side2Marking>250</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>11131-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>11138</Austr>
				<PresentationName>Amoxil</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Amoxycillin trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 13:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red and yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>GS LEX</Side1Marking>
							<Side2Marking>GS LEX</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>11138-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>57574</Austr>
				<PresentationName>Amoxil</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-08 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amoxycillin trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR>97190</IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/10/2008 11:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red and yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>GS JVL</Side1Marking>
							<Side2Marking>GS JVL</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>57574-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amoxycillin (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>142491</Austr>
				<PresentationName>APO-Amoxycillin</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-07-27 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amoxycillin trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/06/2009 09:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>250</Side1Marking>
							<Side2Marking>250</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>142491-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>142538</Austr>
				<PresentationName>APO-Amoxycillin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-07-27 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amoxycillin trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
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						<VersionStatus>current</VersionStatus>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>brown and yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking>500</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>142538-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>208144</Austr>
				<PresentationName>APO-Amoxycillin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amoxycillin trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>maroon/yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>RX655</Side1Marking>
							<Side2Marking>RX655</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>208144-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>208147</Austr>
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    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amoxycillin trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Colour>yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>RX654</Side1Marking>
							<Side2Marking>RX654</Side2Marking>
							<Views>
							<View>
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								<ImageFileName>208147-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Amoxycillin (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>152851</Austr>
				<PresentationName>Amoxycillin generichealth</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>01/10/2012 12:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque brown/yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking>500</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152851-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>207005</Austr>
				<PresentationName>Amoxycillin generichealth</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/08/2017 10:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque maroon/yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>RX655</Side1Marking>
							<Side2Marking>RX655</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>207005-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amoxycillin (GenRx)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>96875</Austr>
				<PresentationName>GenRx Amoxycillin Capsules</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>01/08/2008 09:20</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96875-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>96876</Austr>
				<PresentationName>GenRx Amoxycillin Capsules</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96876-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amoxycillin (GN)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>95456</Austr>
				<PresentationName>GN-Amoxycillin</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/07/2009 14:01</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Capsules</DoseForm>
							<Colour>yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>95457</Austr>
				<PresentationName>GN-Amoxycillin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Capsules</DoseForm>
							<Colour>yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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								<ImageFileName>95457-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amoxycillin (Ranbaxy)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>152852</Austr>
				<PresentationName>Amoxycillin Ranbaxy</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<Scoring></Scoring>
							<Shape></Shape>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>152853</Austr>
				<PresentationName>Amoxycillin Ranbaxy</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
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							<Scoring></Scoring>
							<Shape></Shape>
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							<Views>
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		</Brand><Brand>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
				<Austr>63333</Austr>
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    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amoxycillin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>14/08/2009 15:22</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>98758</Austr>
				<PresentationName>Amoxycillin Sandoz</PresentationName>
    			<PresentionStrength>1g</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amoxycillin trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>24/09/2008 17:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to cream</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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								<ImageFileName>98758-C01-01-BL600.jpg</ImageFileName>
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				</Images>
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		</Brand><Brand>
			<brandname>Amoxycillin and Clavulanic Acid (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>123968</Austr>
				<PresentationName>Amoxyclav AN</PresentationName>
    			<PresentionStrength>500mg/125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>26/07/2017 16:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>123968-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>123971</Austr>
				<PresentationName>Amoxyclav AN</PresentationName>
    			<PresentionStrength>875mg/125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>123971-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Amoxycillin and Clavulanic Acid (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>153775</Austr>
				<PresentationName>Apo-Amoxycillin and Clavulanic Acid</PresentationName>
    			<PresentionStrength>500mg/125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-07-29 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/05/2010 10:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153775-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>163696</Austr>
				<PresentationName>APO-Amoxycillin and Clavulanic Acid 875/125mg</PresentationName>
    			<PresentionStrength>875mg/125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amoxycillin trihydrate,Potassium clavulanate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>875 125</Side1Marking>
							<Side2Marking>AMC</Side2Marking>
							<Views>
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								<ViewLabel>C</ViewLabel>
								<ImageFileName>163696-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>317064</Austr>
				<PresentationName>Amoxycillin and Clavulanic Acid  Apotex</PresentationName>
    			<PresentionStrength>500mg/125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>amoxicillin trihydrate,potassium clavulanate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>24/08/2021 16:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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		</Brand><Brand>
			<brandname>Amoxycillin and Clavulanic Acid (Generic Health)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>82832</Austr>
				<PresentationName>AmoxyClav GH</PresentationName>
    			<PresentionStrength>875mg/125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82832-C01-01-BL600.jpg</ImageFileName>
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		</Brand><Brand>
			<brandname>Amoxycillin and Clavulanic Acid (GenRx)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>81162</Austr>
				<PresentationName>GenRx Amoxycillin and Clavulanic Acid</PresentationName>
    			<PresentionStrength>875mg/125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Potassium clavulanate,Amoxycillin trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/12/2010 12:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>875 125</Side1Marking>
							<Side2Marking>AMC</Side2Marking>
							<Views>
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		</Brand><Brand>
			<brandname>Amoxycillin and Clavulanic Acid (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>196893</Austr>
				<PresentationName>Pharmacor Amoxyclav</PresentationName>
    			<PresentionStrength>875mg/125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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							<Scoring>unscored</Scoring>
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							<Side1Marking></Side1Marking>
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		</Brand><Brand>
			<brandname>Amprace</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>11612</Austr>
				<PresentationName>Amprace</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Enalapril maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>rust-red</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>A 713</Side1Marking>
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			<Presentations>
				<Austr>11613</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Enalapril maleate</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
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							<Shape>round</Shape>
							<Side1Marking>A 714</Side1Marking>
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		</Brand><Brand>
			<brandname>Anafranil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clomipramine hydrochloride</TGAIngredient>
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		</Brand><Brand>
			<brandname>Anagrelide (Apotex)</brandname>
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			<Presentations>
				<Austr>293282</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<brandname>Anamorph</brandname>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
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			<brandname>Anastrozole (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
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				<Austr>158749</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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							<Side1Marking>AHI</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
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			</Presentations>
		</Brand><Brand>
			<brandname>Anastrozole (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>266676</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
							<Side1Marking>1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>266676-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Anastrozole (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>173893</Austr>
				<PresentationName>Chemmart Anastrazole</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
							<Side1Marking>AN 1</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>173893-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Anastrozole (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>155680</Austr>
				<PresentationName>Anastrozole-GA</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>21/06/2012 08:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>A 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>155680-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Anastrozole (Generic Health)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>155177</Austr>
				<PresentationName>Anastrozole GH</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>11/10/2012 11:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ANA 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>155177-C01-01-BL600.jpg</ImageFileName>
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		</Brand><Brand>
			<brandname>Anastrozole (Ranbaxy)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>158253</Austr>
				<PresentationName>Anastrozole RBX</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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							<PhaseItem>1</PhaseItem>
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							<Side1Marking>AHI</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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		</Brand><Brand>
			<brandname>Anastrozole (Sandoz)</brandname>
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			<Presentations>
				<Austr>142746</Austr>
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							<PhaseItem>1</PhaseItem>
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							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
		</Brand><Brand>
			<brandname>Anastrozole (Terry White Chemists)</brandname>
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			<Presentations>
				<Austr>173896</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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							<View>
								<ViewLabel>C</ViewLabel>
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		</Brand><Brand>
			<brandname>Andriol</brandname>
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				<Austr>92904</Austr>
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    			<Container>blister pack</Container>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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							<Side1Marking>LA LA</Side1Marking>
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							<View>
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			<brandname>Angeliq</brandname>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<View>
								<ViewLabel>C</ViewLabel>
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			<brandname>Anpec</brandname>
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   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient>verapamil hydrochloride</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<View>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
		</Brand><Brand>
			<brandname>Antabuse</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>70468</Austr>
				<PresentationName>Antabuse</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CD C</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>70468-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Antenex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>17582</Austr>
				<PresentationName>Antenex</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Diazepam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Antenex</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcanten10822</Filename>
							</AvailableFormats>
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						<ActiveIngredient>diazepam</ActiveIngredient>
						<ReleaseDate>2022-09-07 15:29:53.0</ReleaseDate>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DM 2</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>17582-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>17583</Austr>
				<PresentationName>Antenex</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Diazepam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Antenex</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcanten10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>diazepam</ActiveIngredient>
						<ReleaseDate>2022-09-07 15:29:53.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DM 5</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>17583-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Anterone</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>278777</Austr>
				<PresentationName>Anterone</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 14:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>278777-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>278778</Austr>
				<PresentationName>Anterone</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 14:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>CPA 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>278778-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Anthel</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>17584</Austr>
				<PresentationName>Anthel</PresentationName>
    			<PresentionStrength>125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>17584-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>17585</Austr>
				<PresentationName>Anthel</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>17585-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Antistax</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>171113</Austr>
				<PresentationName>Antistax</PresentationName>
    			<PresentionStrength>360mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
							<Colour>brownish-red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>171113-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Apohealth Anti-inflammatory Pain Relief Tablets</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>287704</Austr>
				<PresentationName>Apohealth Anti-inflammatory Pain Relief Tablets</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>287704-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Apohealth Cold &amp; Flu + Cough Relief Day/Night</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>228149</Austr>
				<PresentationName>Apohealth Cold &amp; Flu + Cough Relief Day/Night</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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							<Shape></Shape>
							<Side1Marking></Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>228149-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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							<DoseForm>Capsules</DoseForm>
							<Colour>red and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>228149-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Apohealth Cold &amp; Flu + Cough Relief PE</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>227350</Austr>
				<PresentationName>Apohealth Cold &amp; Flu + Cough Relief PE</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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							<Shape></Shape>
							<Side1Marking></Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>227350-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Apohealth Cold &amp; Flu Relief PE Day/Night</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>227573</Austr>
				<PresentationName>Apohealth Cold &amp; Flu Relief PE Day/Night</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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							<Side1Marking>D</Side1Marking>
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							<Views>
							<View>
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								<ImageFileName>227573-C01-01-BL600.jpg</ImageFileName>
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							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>caplet-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>227573-C02-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Apohealth Cold Relief</brandname>
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			<Presentations>
				<Austr>254172</Austr>
				<PresentationName>Apohealth Cold Relief</PresentationName>
    			<PresentionStrength>500mg/2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
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							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>254172-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Apohealth Diarrhoea Relief</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>226879</Austr>
				<PresentationName>Apohealth Diarrhoea Relief</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>grey and green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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		</Brand><Brand>
			<brandname>Apohealth Diarrhoea Relief Plus</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>235981</Austr>
				<PresentationName>Apohealth Diarrhoea Relief Plus</PresentationName>
    			<PresentionStrength>2mg/125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white, slightly mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>235981-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>235981-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Apohealth Laxative with Softener</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>229304</Austr>
				<PresentationName>Apohealth Laxative with Softener</PresentationName>
    			<PresentionStrength>50mg/8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/02/2017 12:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>229304-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Apohealth Period Pain Relief</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>230081</Austr>
				<PresentationName>Apohealth Period Pain Relief</PresentationName>
    			<PresentionStrength>275mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/02/2017 13:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>230081-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Apohealth PSE Day + Night Cold &amp; Flu Relief</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>294256</Austr>
				<PresentationName>Apohealth PSE Day + Night Cold &amp; Flu Relief</PresentationName>
    			<PresentionStrength>500mg/30mg/2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/08/2021 16:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>294256-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>294256-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>294256-A02-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>294256-B02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Apohealth Sinus Nasal Decongestant</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>265772</Austr>
				<PresentationName>Apohealth Sinus Nasal Decongestant</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/02/2017 12:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>265772-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Apohealth Sleep Assist</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>254173</Austr>
				<PresentationName>Apohealth Sleep Assist</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/02/2017 12:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>254173-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Apohealth Stomach Ease Forte</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>256532</Austr>
				<PresentationName>Apohealth Stomach Ease Forte</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/02/2017 12:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>256532-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Apohealth Worm Treatment</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>229073</Austr>
				<PresentationName>Apohealth Worm Treatment</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/02/2017 12:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>229073-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Appese</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>140833</Austr>
				<PresentationName>Appese</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 14:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>pentagon-shaped</Shape>
							<Side1Marking>RI 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>140833-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>140835</Austr>
				<PresentationName>Appese</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 14:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>pentagon-shaped</Shape>
							<Side1Marking>RI 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>140835-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aptivus</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>118104</Austr>
				<PresentationName>Aptivus</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>tipranavir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/11/2010 10:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>pink</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>TPV 250</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>118104-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Arabloc</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>92753</Austr>
				<PresentationName>Arabloc</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Leflunomide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Arabloc</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcarabl10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>leflunomide</ActiveIngredient>
						<ReleaseDate>2022-07-14 16:19:04.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/11/2008 08:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to almost white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ZBN</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>92753-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>92754</Austr>
				<PresentationName>Arabloc</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Leflunomide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Arabloc</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>leflunomide</ActiveIngredient>
						<ReleaseDate>2022-07-14 16:19:04.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/11/2008 08:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellowish to ochre</Colour>
							<Scoring>unscored</Scoring>
							<Shape>spherical triangular</Shape>
							<Side1Marking>ZBO</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>92754-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aratac</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>32514</Austr>
				<PresentationName>Aratac</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amiodarone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Aratac</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amiodarone hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-01-25 18:32:31.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/03/2018 12:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AM 200</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>32514-C01-02-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>32519</Austr>
				<PresentationName>Aratac</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amiodarone hydrochloride</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Aratac</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
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						<ReleaseDate>2022-01-25 18:32:31.0</ReleaseDate>
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						<DateEffective>26/10/2016 14:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
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							<Shape>round</Shape>
							<Side1Marking>AM 100</Side1Marking>
							<Side2Marking>G</Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
		</Brand><Brand>
			<brandname>Arava</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>69692</Austr>
				<PresentationName>Arava</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Leflunomide</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<QualiferData></QualiferData>
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						<DocumentTypes>
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						<ActiveIngredient>leflunomide</ActiveIngredient>
						<ReleaseDate>2022-07-14 16:18:44.0</ReleaseDate>
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						<DateEffective>25/06/2008 15:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to almost white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ZBN</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>69692-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>69694</Austr>
				<PresentationName>Arava</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Leflunomide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>25/06/2008 15:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellowish to ochre</Colour>
							<Scoring>unscored</Scoring>
							<Shape>spherical triangular</Shape>
							<Side1Marking>ZBO</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>69694-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>69695</Austr>
				<PresentationName>Arava</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Leflunomide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to almost white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ZBP</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>69695-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Arazil</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>167692</Austr>
				<PresentationName>Arazil</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Donepezil hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Arazil</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>donepezil hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-04-04 14:41:51.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DL 5</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>167693</Austr>
				<PresentationName>Arazil</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Donepezil hydrochloride</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<QualiferData></QualiferData>
						<DocumentName>Arazil</DocumentName>
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						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DL 10</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
		</Brand><Brand>
			<brandname>Arcoxia</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>131797</Austr>
				<PresentationName>Arcoxia</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Etoricoxib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Arcoxia</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcarcox10921</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>etoricoxib</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>17/11/2008 17:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue-green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>apple-shaped</Shape>
							<Side1Marking>ACX 30</Side1Marking>
							<Side2Marking>101</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>81456</Austr>
				<PresentationName>Arcoxia</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Etoricoxib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Arcoxia</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>etoricoxib</ActiveIngredient>
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				<Images>
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						<VersionSequence>1</VersionSequence>
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						<DateEffective>17/11/2008 17:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>apple-shaped</Shape>
							<Side1Marking>ARCOXIA 60</Side1Marking>
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							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>81458</Austr>
				<PresentationName>Arcoxia</PresentationName>
    			<PresentionStrength>120mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Etoricoxib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Scoring>unscored</Scoring>
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							<Side1Marking>ARCOXIA 120</Side1Marking>
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							<Views>
							<View>
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			<brandname>Ardix Gliclazide</brandname>
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			<Presentations>
				<Austr>154049</Austr>
				<PresentationName>Ardix Gliclazide MR</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gliclazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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			<Presentations>
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				<PresentationName>Arianna</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
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							<Views>
							<View>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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				<Documents>
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						<DocumentName>Arianna 1</DocumentName>
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							<AvailableFormats>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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                    	<Phase>
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			<Presentations>
				<Austr>60176</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Aricept</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcarict20122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>donepezil hydrochloride</ActiveIngredient>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/08/2008 10:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ARICEPT</Side1Marking>
							<Side2Marking>5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>60176-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>60178</Austr>
				<PresentationName>Aricept</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Donepezil hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Aricept</DocumentName>
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							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>donepezil hydrochloride</ActiveIngredient>
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				<Images>
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						<DateEffective>19/09/2011 15:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ARICEPT</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>60178-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aridon APN</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167190</Austr>
				<PresentationName>Aridon APN</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 14:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167190-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>167193</Austr>
				<PresentationName>Aridon APN</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 14:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167193-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Arimidex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>54672</Austr>
				<PresentationName>Arimidex</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Anastrozole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Arimidex</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apcarini11121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>anastrozole</ActiveIngredient>
						<ReleaseDate>2021-11-18 15:44:44.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 10:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Adx 1</Side1Marking>
							<Side2Marking>'A' with arrowhead</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>54672-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aripiprazole (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>198195</Austr>
				<PresentationName>Aripiprazole AN</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/03/2019 14:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>H</Side1Marking>
							<Side2Marking>65</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>198195-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>198206</Austr>
				<PresentationName>Aripiprazole AN</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/03/2019 14:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>H</Side1Marking>
							<Side2Marking>64</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>198206-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aripiprazole (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>152899</Austr>
				<PresentationName>APO-Aripiprazole</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/07/2017 15:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ARI 20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152899-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>152904</Austr>
				<PresentationName>APO-Aripiprazole</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/07/2017 15:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rectangular</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152904-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>152905</Austr>
				<PresentationName>APO-Aripiprazole</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/07/2017 15:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ARI 30</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152905-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>152908</Austr>
				<PresentationName>APO-Aripiprazole</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/07/2017 15:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rectangular</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152908-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>152924</Austr>
				<PresentationName>APO-Aripiprazole</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/07/2017 15:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ARI 15</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152924-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aripiprazole (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>158274</Austr>
				<PresentationName>Aripiprazole Sandoz</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 15:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>449</Side1Marking>
							<Side2Marking>SZ</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158274-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158281</Austr>
				<PresentationName>Aripiprazole Sandoz</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>447</Side1Marking>
							<Side2Marking>SZ</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158281-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158283</Austr>
				<PresentationName>Aripiprazole Sandoz</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>446</Side1Marking>
							<Side2Marking>SZ</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158283-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158285</Austr>
				<PresentationName>Aripiprazole Sandoz</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>448</Side1Marking>
							<Side2Marking>SZ</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158285-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aromasin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>76369</Austr>
				<PresentationName>Aromasin</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Exemestane</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Aromasin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcaromt11121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>exemestane</ActiveIngredient>
						<ReleaseDate>2021-12-03 13:32:41.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/09/2011 15:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white to slightly greyish</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>7663</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>76369-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aropax</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>57927</Austr>
				<PresentationName>Aropax</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Paroxetine hydrochloride hemihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/03/2012 15:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>57927-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Artane</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>15125</Austr>
				<PresentationName>Artane</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/03/2010 11:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>15125-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>15126</Austr>
				<PresentationName>Artane</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 14:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>15126-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Arthrexin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>17586</Austr>
				<PresentationName>Arthrexin</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Indomethacin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>IN-25</Side1Marking>
							<Side2Marking>IN-25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>17586-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Artige</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>117306</Austr>
				<PresentationName>Artige</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>methylphenidate hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Artige</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcartor10422</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>methylphenidate hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-04-13 08:34:47.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/07/2021 15:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AB</Side1Marking>
							<Side2Marking>CG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>117306-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aspalgin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>13431</Austr>
				<PresentationName>Aspalgin</PresentationName>
    			<PresentionStrength>300mg/8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>codeine phosphate hemihydrate,aspirin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Aspalgin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocaspal10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>aspirin and codeine phosphate hemihydrate</ActiveIngredient>
						<ReleaseDate>2022-05-03 08:07:08.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/12/2021 12:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>FM</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>13431-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>13431-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aspirin (Apohealth)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>229733</Austr>
				<PresentationName>Apohealth Cardio Aspirin</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/02/2017 12:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>heart shape</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>229733-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aspirin (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>190572</Austr>
				<PresentationName>Pharmacy Action Low Dose Aspirin</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>heart shape</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>190572-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aspirin (Mayne Pharma)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>194209</Austr>
				<PresentationName>Mayne Pharma Aspirin</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/06/2017 11:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>heart shape</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>194209-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aspro</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>58566</Austr>
				<PresentationName>Aspro Clear</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2009 15:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>58566-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>58566-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>66381</Austr>
				<PresentationName>Aspro</PresentationName>
    			<PresentionStrength>320mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2009 15:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ASPRO-</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>66381-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>77594</Austr>
				<PresentationName>Aspro Clear Extra Strength</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2009 15:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>77594-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>77594-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Astrix</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>194208</Austr>
				<PresentationName>Astrix</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/06/2017 11:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>heart shape</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>194208-C01-01-BL600.jpg</ImageFileName>
							</View>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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							<Colour>pink</Colour>
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							<Side1Marking>A CH</Side1Marking>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>154247</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient>Hydrochlorothiazide,Candesartan cilexetil</TGAIngredient>
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					</Versions>
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			</Presentations>
			<Presentations>
				<Austr>154251</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>76646</Austr>
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    			<PresentionStrength>16/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			</Presentations>
		</Brand><Brand>
			<brandname>Ataris</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>164963</Austr>
				<PresentationName>Ataris</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			</Presentations>
			<Presentations>
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							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214939-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Atenolol (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>214942</Austr>
				<PresentationName>Chemmart Atenolol </PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atenolol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/05/2017 10:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214942-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Atenolol (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>201777</Austr>
				<PresentationName>Atenolol GH</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/04/2017 15:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ATENOLOL 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>201777-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Atenolol (GenRx)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>129863</Austr>
				<PresentationName>GenRx Atenolol</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atenolol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/10/2008 09:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ATE 50</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>129863-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Atenolol (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>101462</Austr>
				<PresentationName>Atenolol Sandoz</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atenolol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/09/2008 17:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101462-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Atenolol (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>214941</Austr>
				<PresentationName>Terry White Chemists Atenolol</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atenolol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/09/2018 12:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214941-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Atomerra</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>234793</Austr>
				<PresentationName>Atomerra</PresentationName>
    			<PresentionStrength>18mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 14:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>18 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234793-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>234799</Austr>
				<PresentationName>Atomerra</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 14:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>10 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234799-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>234808</Austr>
				<PresentationName>Atomerra</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 14:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light blue and yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>60 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234808-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>234811</Austr>
				<PresentationName>Atomerra</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 14:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>brown</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>100 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234811-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>234813</Austr>
				<PresentationName>Atomerra</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 14:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>25 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234813-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>234814</Austr>
				<PresentationName>Atomerra</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 14:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>40 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234814-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>234815</Austr>
				<PresentationName>Atomerra</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/04/2018 12:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>brown and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>80 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234815-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Atomoxetine (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>238335</Austr>
				<PresentationName>Atomoxetine Amneal</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A910</Side1Marking>
							<Side2Marking>A910</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>238335-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>238336</Austr>
				<PresentationName>Atomoxetine Amneal</PresentationName>
    			<PresentionStrength>18mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>gold opaque and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A918</Side1Marking>
							<Side2Marking>A918</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>238336-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>238337</Austr>
				<PresentationName>Atomoxetine Amneal</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue opaque and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A925</Side1Marking>
							<Side2Marking>A925</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>238337-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>238338</Austr>
				<PresentationName>Atomoxetine Amneal</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A940</Side1Marking>
							<Side2Marking>A940</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>238338-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>238339</Austr>
				<PresentationName>Atomoxetine Amneal</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue opaque and gold opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A960</Side1Marking>
							<Side2Marking>A960</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>238339-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>238340</Austr>
				<PresentationName>Atomoxetine Amneal</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>brown opaque and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A980</Side1Marking>
							<Side2Marking>A980</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>238340-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>238341</Austr>
				<PresentationName>Atomoxetine Amneal</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>brown opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A900</Side1Marking>
							<Side2Marking>A900</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>238341-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Atomoxetine (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>290979</Austr>
				<PresentationName>APO-Atomoxetine</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atomoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/11/2018 19:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>AM10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>290979-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>290980</Austr>
				<PresentationName>APO-Atomoxetine</PresentationName>
    			<PresentionStrength>18mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atomoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/11/2018 19:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>gold and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>AM18</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>290980-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>290981</Austr>
				<PresentationName>APO-Atomoxetine</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atomoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/04/2019 18:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>AM25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>290981-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>290982</Austr>
				<PresentationName>APO-Atomoxetine</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atomoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/11/2018 19:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>AM40</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>290982-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>290983</Austr>
				<PresentationName>APO-Atomoxetine</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atomoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/11/2018 19:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue and gold opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>AM60</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>290983-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>290984</Austr>
				<PresentationName>APO-Atomoxetine</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atomoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/11/2018 19:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>AM80</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>290984-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>290985</Austr>
				<PresentationName>APO-Atomoxetine</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atomoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/11/2018 19:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>AM100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>290985-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Atomoxetine (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>238366</Austr>
				<PresentationName>Atomoxetine Sandoz</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/01/2018 11:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A910</Side1Marking>
							<Side2Marking>A910</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>238366-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>238367</Austr>
				<PresentationName>Atomoxetine Sandoz</PresentationName>
    			<PresentionStrength>18mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/01/2018 11:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>gold opaque and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A918</Side1Marking>
							<Side2Marking>A918</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>238367-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>238368</Austr>
				<PresentationName>Atomoxetine Sandoz</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/01/2018 11:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue opaque and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A925</Side1Marking>
							<Side2Marking>A925</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>238368-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>238369</Austr>
				<PresentationName>Atomoxetine Sandoz</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/01/2018 11:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A940</Side1Marking>
							<Side2Marking>A940</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>238369-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>238370</Austr>
				<PresentationName>Atomoxetine Sandoz</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/01/2018 11:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue opaque and gold opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A960</Side1Marking>
							<Side2Marking>A960</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>238370-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>238371</Austr>
				<PresentationName>Atomoxetine Sandoz</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/01/2018 11:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>brown opaque and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A980</Side1Marking>
							<Side2Marking>A980</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>238371-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>238372</Austr>
				<PresentationName>Atomoxetine Sandoz</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/01/2018 11:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>brown opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A900</Side1Marking>
							<Side2Marking>A900</Side2Marking>
							<Views>
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		</Brand><Brand>
			<brandname>Atorvachol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>178524</Austr>
				<PresentationName>Atorvachol</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>178524-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>178525</Austr>
				<PresentationName>Atorvachol</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>25/11/2013 10:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>178525-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>178535</Austr>
				<PresentationName>Atorvachol</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<DateEffective>25/11/2013 10:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>178535-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>178542</Austr>
				<PresentationName>Atorvachol</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 10:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>178542-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Atorvastatin (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>153718</Austr>
				<PresentationName>APO-Atorvastatin</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium propylene glycol solvate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>A10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153718-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>153729</Austr>
				<PresentationName>APO-Atorvastatin</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium propylene glycol solvate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>ATV80</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153729-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>153732</Austr>
				<PresentationName>APO-Atorvastatin</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium propylene glycol solvate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>ATV20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153732-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>153738</Austr>
				<PresentationName>APO-Atorvastatin</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium propylene glycol solvate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>ATV40</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153738-C01-02-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>286636</Austr>
				<PresentationName>APO-Atorvastatin</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/11/2017 11:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>AS10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>286637</Austr>
				<PresentationName>APO-Atorvastatin</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 12:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>AS20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>286638</Austr>
				<PresentationName>APO-Atorvastatin</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/11/2017 11:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>AS40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>286638-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>286639</Austr>
				<PresentationName>APO-Atorvastatin</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/11/2017 11:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>AS80</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
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				<PresentationName>Blooms the Chemist Atorvastatin</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium propylene glycol solvate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>A10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153717-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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			<Presentations>
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				<PresentationName>Blooms the Chemist Atorvastatin</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium propylene glycol solvate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>ATV80</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153719-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>153722</Austr>
				<PresentationName>Blooms the Chemist Atorvastatin</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium propylene glycol solvate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>ATV40</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153722-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>153736</Austr>
				<PresentationName>Blooms the Chemist Atorvastatin</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium propylene glycol solvate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>ATV20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153736-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>286640</Austr>
				<PresentationName>Blooms the Chemist Atorvastatin</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 12:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>AS10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>286640-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>286642</Austr>
				<PresentationName>Blooms the Chemist Atorvastatin</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 12:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>AS40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>286642-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>286643</Austr>
				<PresentationName>Blooms the Chemist Atorvastatin</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 12:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>AS80</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>286643-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Atorvastatin (Generic Health)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>180320</Austr>
				<PresentationName>Atorvastatin GH</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>180320-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>180321</Austr>
				<PresentationName>Atorvastatin GH</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>180321-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>180326</Austr>
				<PresentationName>Atorvastatin GH</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>180326-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>180330</Austr>
				<PresentationName>Atorvastatin GH</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>180330-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Atorvastatin (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>156051</Austr>
				<PresentationName>Atorvastatin Sandoz</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>HLA 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156051-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156055</Austr>
				<PresentationName>Atorvastatin Sandoz</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to almost white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>HLA 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156055-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156057</Austr>
				<PresentationName>Atorvastatin Sandoz</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>HLA 80</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156057-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156058</Austr>
				<PresentationName>Atorvastatin Sandoz</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>HLA 40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156058-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179823</Austr>
				<PresentationName>Atorvastatin SZ</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/04/2014 14:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>AS40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179823-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179833</Austr>
				<PresentationName>Atorvastatin SZ</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/04/2014 14:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>AS80</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179833-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179842</Austr>
				<PresentationName>Atorvastatin SZ</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>AS20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179842-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179845</Austr>
				<PresentationName>Atorvastatin SZ</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/04/2014 14:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>AS10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179845-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Atozet</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>216956</Austr>
				<PresentationName>Atozet</PresentationName>
    			<PresentionStrength>10mg/20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ezetimibe,Atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Atozet</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
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						</DocumentTypes>
						<ActiveIngredient>ezetimibe with atorvastatin calcium</ActiveIngredient>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>333</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216956-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216958</Austr>
				<PresentationName>Atozet</PresentationName>
    			<PresentionStrength>10mg/40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ezetimibe,Atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Atozet</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcatofd10121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ezetimibe with atorvastatin calcium</ActiveIngredient>
						<ReleaseDate>2021-04-15 11:28:41.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/03/2016 09:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>337</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216958-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216961</Austr>
				<PresentationName>Atozet</PresentationName>
    			<PresentionStrength>10mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ezetimibe,Atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Atozet</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcatofd10121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ezetimibe with atorvastatin calcium</ActiveIngredient>
						<ReleaseDate>2021-04-15 11:28:41.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/03/2016 09:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>257</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216961-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216962</Austr>
				<PresentationName>Atozet</PresentationName>
    			<PresentionStrength>10mg/80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium trihydrate,Ezetimibe</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Atozet</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcatofd10121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ezetimibe with atorvastatin calcium</ActiveIngredient>
						<ReleaseDate>2021-04-15 11:28:41.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/03/2016 09:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>357</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216962-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aubagio</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>192672</Austr>
				<PresentationName>Aubagio</PresentationName>
    			<PresentionStrength>14mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Teriflunomide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Aubagio</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcaubag10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>teriflunomide</ActiveIngredient>
						<ReleaseDate>2022-02-09 14:51:51.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/05/2021 08:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale blue to pastel blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>pentagonal</Shape>
							<Side1Marking>14</Side1Marking>
							<Side2Marking>logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192672-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Augmentin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>142692</Austr>
				<PresentationName>Augmentin Duo</PresentationName>
    			<PresentionStrength>500mg/125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clavulanic acid,Amoxycillin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/10/2008 14:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>A C</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>142692-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>54900</Austr>
				<PresentationName>Augmentin Duo Forte</PresentationName>
    			<PresentionStrength>875mg/125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clavulanic acid,Amoxycillin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 13:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>A C</Side1Marking>
							<Side2Marking>A C</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>54900-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aurorix</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>51626</Austr>
				<PresentationName>Aurorix</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Moclobemide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Aurorix</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocauror10322</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>moclobemide</ActiveIngredient>
						<ReleaseDate>2022-03-21 09:37:11.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/06/2012 09:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to yellow-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>51626-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>9987</Austr>
				<PresentationName>Aurorix</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Moclobemide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Aurorix</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocauror10322</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>moclobemide</ActiveIngredient>
						<ReleaseDate>2022-03-21 09:37:11.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/09/2013 09:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>9987-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Auscap</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>140589</Austr>
				<PresentationName>Auscap</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/03/2010 11:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light green and ivory</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>140589-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ausfam</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>93788</Austr>
				<PresentationName>Ausfam</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 14:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>tan</Colour>
							<Scoring>unscored</Scoring>
							<Shape>square</Shape>
							<Side1Marking>FO 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>93788-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>93789</Austr>
				<PresentationName>Ausfam</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 14:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>square</Shape>
							<Side1Marking>FO 40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>93789-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ausgem</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>62099</Austr>
				<PresentationName>Ausgem</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 14:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62099-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Auspril</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>121756</Austr>
				<PresentationName>Auspril</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>EL 20</Side1Marking>
							<Side2Marking>Arrow logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121756-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121757</Austr>
				<PresentationName>Auspril</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brownish-pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>EL 10</Side1Marking>
							<Side2Marking>Arrow logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121757-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>77035</Austr>
				<PresentationName>Auspril</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ELP 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>77035-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ausran</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>97354</Austr>
				<PresentationName>Ausran</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 14:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>97354-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>97355</Austr>
				<PresentationName>Ausran</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/02/2018 14:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>97355-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Avanza</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>121868</Austr>
				<PresentationName>Avanza</PresentationName>
    			<PresentionStrength>45mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/10/2010 11:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>TZ 7</Side1Marking>
							<Side2Marking>Organon</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121868-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>77115</Austr>
				<PresentationName>Avanza</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Avanza</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcavant10121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>mirtazapine</ActiveIngredient>
						<ReleaseDate>2021-04-15 11:37:52.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/10/2010 11:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red-brown</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>TZ 5 TZ 5</Side1Marking>
							<Side2Marking>Organon</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>77115-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Avapro</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>101730</Austr>
				<PresentationName>Avapro</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Avapro</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcavapr10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>irbesartan</ActiveIngredient>
						<ReleaseDate>2022-08-30 17:44:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/07/2013 10:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>2871</Side1Marking>
							<Side2Marking>heart shape</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101730-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101734</Austr>
				<PresentationName>Avapro</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Avapro</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcavapr10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>irbesartan</ActiveIngredient>
						<ReleaseDate>2022-08-30 17:44:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/07/2013 10:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>2872</Side1Marking>
							<Side2Marking>heart shape</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101734-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101736</Austr>
				<PresentationName>Avapro</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Avapro</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcavapr10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>irbesartan</ActiveIngredient>
						<ReleaseDate>2022-08-30 17:44:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/07/2013 10:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>2873</Side1Marking>
							<Side2Marking>heart shape</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101736-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Avapro HCT</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>102017</Austr>
				<PresentationName>Avapro HCT</PresentationName>
    			<PresentionStrength>150mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Avapro HCT</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcavhct10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>irbesartan with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2022-09-07 16:29:29.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/07/2013 10:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>2875</Side1Marking>
							<Side2Marking>heart shape</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>102017-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>102086</Austr>
				<PresentationName>Avapro HCT</PresentationName>
    			<PresentionStrength>300mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Avapro HCT</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcavhct10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>irbesartan with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2022-09-07 16:29:29.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/07/2013 10:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>2876</Side1Marking>
							<Side2Marking>heart shape</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>102086-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>129436</Austr>
				<PresentationName>Avapro HCT</PresentationName>
    			<PresentionStrength>300mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Avapro HCT</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcavhct10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>irbesartan with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2022-09-07 16:29:29.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/07/2013 10:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>2788</Side1Marking>
							<Side2Marking>heart shape</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>129436-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Avelox</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>75766</Austr>
				<PresentationName>Avelox</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/04/2010 10:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dull red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>M400</Side1Marking>
							<Side2Marking>BAYER</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75766-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Avodart</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>90434</Austr>
				<PresentationName>Avodart</PresentationName>
    			<PresentionStrength>500mcg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Dutasteride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Avodart</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gwcavoda10513</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>dutasteride</ActiveIngredient>
						<ReleaseDate>2013-08-09 09:23:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/09/2009 14:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque yellow</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>GX CE2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>90434-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Avsartan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>268772</Austr>
				<PresentationName>Avsartan</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/10/2018 15:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>268772-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>268774</Austr>
				<PresentationName>Avsartan</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/10/2018 16:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>268774-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>268780</Austr>
				<PresentationName>Avsartan</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/10/2018 16:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>75</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>268780-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Avsartan HCT</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>272655</Austr>
				<PresentationName>Avsartan HCT</PresentationName>
    			<PresentionStrength>150mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/10/2018 16:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>IH</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>272655-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>272659</Austr>
				<PresentationName>Avsartan HCT</PresentationName>
    			<PresentionStrength>300mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/10/2018 16:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>IH2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>272659-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>272662</Austr>
				<PresentationName>Avsartan HCT</PresentationName>
    			<PresentionStrength>300mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/10/2018 16:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brick red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>IH1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>272662-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Axit</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>164493</Austr>
				<PresentationName>Axit</PresentationName>
    			<PresentionStrength>45mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Axit</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcaxit_10221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>mirtazapine</ActiveIngredient>
						<ReleaseDate>2021-02-12 14:59:23.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/07/2011 13:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>MR 45</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>164493-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>97194</Austr>
				<PresentationName>Axit</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Axit</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcaxit_10221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>mirtazapine</ActiveIngredient>
						<ReleaseDate>2021-02-12 14:59:23.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2009 13:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>MR 15</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>97194-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>97195</Austr>
				<PresentationName>Axit</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Axit</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcaxit_10221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>mirtazapine</ActiveIngredient>
						<ReleaseDate>2021-02-12 14:59:23.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>buff</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>MR 30</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>97195-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Aylide</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>116858</Austr>
				<PresentationName>Aylide</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Glimepiride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>GM 1</Side1Marking>
							<Side2Marking>G G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>116858-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>116859</Austr>
				<PresentationName>Aylide</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Glimepiride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>GM 2</Side1Marking>
							<Side2Marking>G G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>116859-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>116860</Austr>
				<PresentationName>Aylide</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Glimepiride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>GM 3</Side1Marking>
							<Side2Marking>G G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>116860-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>116862</Austr>
				<PresentationName>Aylide</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Glimepiride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>GM 4</Side1Marking>
							<Side2Marking>G G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>116862-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Azamun</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>64490</Austr>
				<PresentationName>Azamun</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 11:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AZA 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>64490-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Azapin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>92801</Austr>
				<PresentationName>Azapin</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AZA 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>92801-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Azathioprine (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>184936</Austr>
				<PresentationName>Azathioprine AN</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>26/07/2017 16:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>AZA 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184936-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
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			</Presentations>
		</Brand><Brand>
			<brandname>Azathioprine (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>205759</Austr>
				<PresentationName>APO-Azathioprine </PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Azathioprine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>10/09/2014 10:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AZA 25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>205759-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>205762</Austr>
				<PresentationName>APO-Azathioprine </PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Azathioprine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/12/2016 19:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AZA 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>205762-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Azathioprine (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>219041</Austr>
				<PresentationName>Azathioprine GH</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>03/05/2017 14:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to yellowish white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>219041-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>219042</Austr>
				<PresentationName>Azathioprine GH</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>03/05/2017 14:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to yellowish white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>219042-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Azathioprine (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>74404</Austr>
				<PresentationName>Azathioprine Sandoz</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Azathioprine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 14:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to yellowish white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>74404-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>74407</Austr>
				<PresentationName>Azathioprine Sandoz</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Azathioprine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 11:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to yellowish-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>74407-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Azilect</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>170172</Austr>
				<PresentationName>Azilect</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rasagiline</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Azilect </DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcazile10608</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>rasagiline mesilate</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/06/2012 09:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>GIL 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>170172-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Azithromycin (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>195910</Austr>
				<PresentationName>APO-Azithromycin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Azithromycin dihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/08/2013 09:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>AZ500</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195910-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Azithromycin (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>195916</Austr>
				<PresentationName>Chemmart Azithromycin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Azithromycin dihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>AZ500</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195916-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Azithromycin (Mylan)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>158290</Austr>
				<PresentationName>Azithromycin Mylan</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>azithromycin dihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Azithromycin Mylan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>azithromycin</ActiveIngredient>
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						<DateEffective>02/05/2019 08:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>A 500</Side1Marking>
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							<Views>
							<View>
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								<ImageFileName>158290-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Azithromycin (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>158292</Austr>
				<PresentationName>Azithromycin Sandoz</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Azithromycin dihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateEffective>26/04/2012 16:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
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							<Side1Marking>A 500</Side1Marking>
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							<Views>
							<View>
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			<brandname>Azithromycin (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>195918</Austr>
				<PresentationName>Terry White Chemists Azithromycin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
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   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient>Azithromycin dihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>AZ500</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
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								<ImageFileName>195918-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Baclofen (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>77576</Austr>
				<PresentationName>APO-Baclofen</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Baclofen</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
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							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>77577</Austr>
				<PresentationName>APO-Baclofen</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Baclofen</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>APO B10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>77577-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Bactrim</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>162563</Austr>
				<PresentationName>Bactrim DS</PresentationName>
    			<PresentionStrength>160/800mg</PresentionStrength>
    			<PresentationForm>DS Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Trimethoprim,Sulfamethoxazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/11/2010 11:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>DS Tablets</DoseForm>
							<Colour>white to almost white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>ROCHE 800 + 160</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>162563-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Belsomra</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>207709</Austr>
				<PresentationName>Belsomra</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>suvorexant</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Belsomra</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>mkcbelso10920</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>suvorexant</ActiveIngredient>
						<ReleaseDate>2020-09-24 14:28:11.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/11/2019 10:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>325</Side1Marking>
							<Side2Marking>MSD logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>207709-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>207712</Austr>
				<PresentationName>Belsomra</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>suvorexant</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Belsomra</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>mkcbelso10920</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>suvorexant</ActiveIngredient>
						<ReleaseDate>2020-09-24 14:28:11.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/11/2019 10:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>MSD logo 335</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>207712-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Benztrop</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>83130</Austr>
				<PresentationName>Benztrop</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/01/2010 15:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PMS 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>83130-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Berocca Performance</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>129630</Austr>
				<PresentationName>Berocca Performance Tropical</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/02/2010 10:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow and orange speckled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>129630-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>129630-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>129631</Austr>
				<PresentationName>Berocca Performance Original</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2009 14:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink and white speckled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>129631-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>129631-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>81974</Austr>
				<PresentationName>Berocca Performance Orange</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/02/2010 10:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange and red speckled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>81974-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>81974-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>82484</Austr>
				<PresentationName>Berocca Performance</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/02/2010 10:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82484-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Betahistine dihydrochloride (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>163021</Austr>
				<PresentationName>Betahistine AN</PresentationName>
    			<PresentionStrength>16mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/11/2017 16:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>163021-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Betahistine dihydrochloride (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>217105</Austr>
				<PresentationName>APO-Betahistine</PresentationName>
    			<PresentionStrength>16mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Betahistine dihydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white or almost white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>B 16</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>217105-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Betahistine dihydrochloride (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>212076</Austr>
				<PresentationName>Betahistine GH</PresentationName>
    			<PresentionStrength>16mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/04/2017 15:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to light creamy</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>212076-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Betahistine dihydrochloride (Viatris)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>286806</Austr>
				<PresentationName>Betahistine Viatris Tablets</PresentationName>
    			<PresentionStrength>16mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>betahistine dihydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Betahistine Viatris</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>betahistidine dihydrochloride</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 14:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>267 267</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>286806-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Betaloc</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>12065</Austr>
				<PresentationName>Betaloc Tablets</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metoprolol tartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Betaloc Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apcbetat11117</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>metoprolol tartrate</ActiveIngredient>
						<ReleaseDate>2017-11-24 16:05:30.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 11:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>A BB</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>12065-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>12384</Austr>
				<PresentationName>Betaloc Tablets</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metoprolol tartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Betaloc Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>metoprolol tartrate</ActiveIngredient>
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					</DocumentQualifiers>
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    			<Container>blister pack</Container>
    			<TGAIngredient>Bisoprolol fumarate</TGAIngredient>
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						<QualiferData></QualiferData>
						<DocumentName>Bicor</DocumentName>
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							<PhaseItem>1</PhaseItem>
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							<Side2Marking></Side2Marking>
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			<Presentations>
				<Austr>81608</Austr>
				<PresentationName>Bicor</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bisoprolol fumarate</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Side2Marking></Side2Marking>
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			<brandname>Biltricide</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>18845</Austr>
				<PresentationName>Biltricide</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>30/04/2010 15:20</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
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							<Side1Marking>L G</Side1Marking>
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			</Presentations>
		</Brand><Brand>
			<brandname>Bisacodyl (Apohealth)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>267256</Austr>
				<PresentationName>Apohealth Bisacodyl Laxative</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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						<DateEffective>07/02/2017 12:08</DateEffective>
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							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
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							<Side2Marking></Side2Marking>
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		</Brand><Brand>
			<brandname>Bisacodyl (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>232022</Austr>
				<PresentationName>Pharmacy Action Pharmalax</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>03/05/2017 14:42</DateEffective>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
		</Brand><Brand>
			<brandname>Bisalax</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>72491</Austr>
				<PresentationName>Bisalax</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
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					<Versions>
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							<Views>
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			<brandname>Biso</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>164255</Austr>
				<PresentationName>Biso 5</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>25/11/2013 10:13</DateEffective>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
							<Side1Marking>BI 5</Side1Marking>
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							<Views>
							<View>
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			<Presentations>
				<Austr>164256</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>mottled beige</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>BI 10</Side1Marking>
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							<View>
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			<Presentations>
				<Austr>164259</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>BI 2.5</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>164259-C01-01-BL600.jpg</ImageFileName>
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		</Brand><Brand>
			<brandname>Bisolvon Chesty</brandname>
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			<Presentations>
				<Austr>125375</Austr>
				<PresentationName>Bisolvon Chesty Forte</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
				<Austr>175930</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<brandname>Bisoprolol fumarate (Apotex)</brandname>
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			<Presentations>
				<Austr>182106</Austr>
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			<Presentations>
				<Austr>182114</Austr>
				<PresentationName>APO-Bisoprolol</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bisoprolol fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/07/2012 11:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>182114-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>182123</Austr>
				<PresentationName>APO-Bisoprolol</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bisoprolol fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/07/2012 11:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>182123-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Bisoprolol fumarate (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>182111</Austr>
				<PresentationName>Chemmart Bisoprolol</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bisoprolol fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/07/2012 14:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>182111-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>182118</Austr>
				<PresentationName>Chemmart Bisoprolol</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bisoprolol fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/07/2012 14:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>2 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>182118-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>182125</Austr>
				<PresentationName>Chemmart Bisoprolol</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bisoprolol fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/07/2012 14:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>182125-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Bisoprolol fumarate (Generic Health)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>212058</Austr>
				<PresentationName>Bisoprolol generichealth</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/04/2017 15:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale orange - light orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>heart-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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								<ImageFileName>212058-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
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			</Presentations>
			<Presentations>
				<Austr>212062</Austr>
				<PresentationName>Bisoprolol generichealth</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white-yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>heart-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>212063</Austr>
				<PresentationName>Bisoprolol generichealth</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>24/04/2017 15:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>heart-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Bisoprolol fumarate (Sandoz)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>144867</Austr>
				<PresentationName>Bisoprolol Sandoz</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bisoprolol fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>28/05/2012 11:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>BIS 2.5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>144884</Austr>
				<PresentationName>Bisoprolol Sandoz</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bisoprolol fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>BIS 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>144888</Austr>
				<PresentationName>Bisoprolol Sandoz</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bisoprolol fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 11:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>light orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>BIS 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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			</Presentations>
		</Brand><Brand>
			<brandname>Bisoprolol fumarate (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>182115</Austr>
				<PresentationName>Terry White Chemists Bisoprolol</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bisoprolol fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>2 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>182120</Austr>
				<PresentationName>Terry White Chemists Bisoprolol</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bisoprolol fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>182122</Austr>
				<PresentationName>Terry White Chemists Bisoprolol</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bisoprolol fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
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							<Side1Marking>5</Side1Marking>
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							<Views>
							<View>
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						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Bispro</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>130178</Austr>
				<PresentationName>Bispro</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bisoprolol fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Bispro</DocumentName>
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								<Format>PDF</Format>
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						<ActiveIngredient>bisoprolol fumarate</ActiveIngredient>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
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			</Presentations>
			<Presentations>
				<Austr>130180</Austr>
				<PresentationName>Bispro</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bisoprolol fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>119673</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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		</Brand><Brand>
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				<Austr>181921</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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							<Side1Marking>L 134</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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			<Presentations>
				<Austr>66704</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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							<Side2Marking></Side2Marking>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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							<View>
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			<isamtbrand>true</isamtbrand>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
				<Austr>257754</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			<isamtbrand>true</isamtbrand>
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				<Austr>206776</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>tiotropium bromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Braltus</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcbralt10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tiotropium bromide monohydrate</ActiveIngredient>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/09/2022 11:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>colourless and transparent</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>293317-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Brenda</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>55128</Austr>
				<PresentationName>Brenda-35 ED</PresentationName>
    			<PresentionStrength>28</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Cyproterone acetate,Ethinyloestradiol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Brenda-35 ED</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>cyproterone acetate with ethinylestradiol</ActiveIngredient>
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						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>55128-C01-01-BL600.jpg</ImageFileName>
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							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>55128-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Brevinor</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10045</Austr>
				<PresentationName>Brevinor-1</PresentationName>
    			<PresentionStrength>1mg/35mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ethinyloestradiol,Norethisterone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/08/2008 11:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>BX</Side1Marking>
							<Side2Marking>SEARLE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10045-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>62131</Austr>
				<PresentationName>Brevinor</PresentationName>
    			<PresentionStrength>500mcg/35mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ethinyloestradiol,Norethisterone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/08/2008 11:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>BX</Side1Marking>
							<Side2Marking>SEARLE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62131-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>62132</Austr>
				<PresentationName>Brevinor </PresentationName>
    			<PresentionStrength>500mcg/35mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ethinyloestradiol,Norethisterone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Brevinor</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>norethisterone with ethinylestradiol</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/09/2008 14:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>BX</Side1Marking>
							<Side2Marking>SEARLE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>P</Side1Marking>
							<Side2Marking>SEARLE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62132-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>62134</Austr>
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    			<PresentionStrength>1mg/35mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ethinyloestradiol,Norethisterone</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>19/09/2011 16:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
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							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>P</Side1Marking>
							<Side2Marking>SEARLE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62134-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Brilinta</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167237</Austr>
				<PresentationName>Brilinta</PresentationName>
    			<PresentionStrength>90mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ticagrelor</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Brilinta</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>ticagrelor</ActiveIngredient>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>02/03/2012 10:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>90 T</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167237-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>303878</Austr>
				<PresentationName>Brilinta</PresentationName>
    			<PresentionStrength>90mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>ticagrelor</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Brilinta</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>ticagrelor</ActiveIngredient>
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				<Images>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/02/2020 14:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
							<Side1Marking>90 TI</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
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							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>303878-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Brintellix</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>203955</Austr>
				<PresentationName>Brintellix</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Vortioxetine hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Brintellix</DocumentName>
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						<ActiveIngredient>vortioxetine hydrobromide</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/07/2015 11:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>almond-shaped</Shape>
							<Side1Marking>TL</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>203970</Austr>
				<PresentationName>Brintellix</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Vortioxetine hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Brintellix</DocumentName>
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						<ActiveIngredient>vortioxetine hydrobromide</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/06/2015 15:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>almond-shaped</Shape>
							<Side1Marking>TL</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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				</Images>
			</Presentations>
			<Presentations>
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				<PresentationName>Brintellix</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Vortioxetine hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Brintellix</DocumentName>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>almond-shaped</Shape>
							<Side1Marking>TL</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			<Presentations>
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				<PresentationName>Brintellix</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Vortioxetine hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Brintellix</DocumentName>
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						</DocumentTypes>
						<ActiveIngredient>vortioxetine hydrobromide</ActiveIngredient>
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						<DateEffective>30/06/2015 15:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>almond-shaped</Shape>
							<Side1Marking>TL</Side1Marking>
							<Side2Marking>5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>203986-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Briviact</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>243792</Austr>
				<PresentationName>Briviact</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/02/2020 10:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green-grey</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>u100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>243792-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>243796</Austr>
				<PresentationName>Briviact</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/02/2020 10:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>grey</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>u25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>243796-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>243797</Austr>
				<PresentationName>Briviact</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/02/2020 10:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>u50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>243797-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>243798</Austr>
				<PresentationName>Briviact</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/02/2020 10:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>purple</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>u75</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>243798-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Brufen</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>80659</Austr>
				<PresentationName>Brufen</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ibuprofen</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Brufen Tablets</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocbrufn11021</Filename>
							</AvailableFormats>
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						<ActiveIngredient>ibuprofen</ActiveIngredient>
						<ReleaseDate>2021-10-14 07:03:09.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/11/2008 08:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>pillow-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>80659-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Brufen Plus</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>298439</Austr>
				<PresentationName>Brufen Plus</PresentationName>
    			<PresentionStrength>200mg/12.8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ibuprofen,codeine phosphate hemihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Brufen Plus 200/12.8</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ibuprofen with codeine phosphate hemihydrate</ActiveIngredient>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>31/01/2022 15:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>298439-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Burinex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>51734</Austr>
				<PresentationName>Burinex</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bumetanide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>11/08/2008 12:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>1 mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>51734-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Buscopan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>153552</Austr>
				<PresentationName>Buscopan Forte</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>hyoscine butylbromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Buscopan Forte</DocumentName>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>hyoscine butylbromide</ActiveIngredient>
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				<Images>
					<Versions>
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						<DateEffective>27/07/2010 10:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>B</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153552-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>48256</Austr>
				<PresentationName>Buscopan</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hyoscine butylbromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Buscopan 10mg tablets</DocumentName>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>hyoscine butylbromide</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/07/2010 10:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>48256-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>C-Flox</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>195202</Austr>
				<PresentationName>C-Flox</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ciprofloxacin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>C-Flox</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ciprofloxacin</ActiveIngredient>
						<ReleaseDate>2022-08-08 13:27:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CF 250</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195202-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>195203</Austr>
				<PresentationName>C-Flox</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ciprofloxacin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>C-Flox</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccflox10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ciprofloxacin</ActiveIngredient>
						<ReleaseDate>2022-08-08 13:27:55.0</ReleaseDate>
					</DocumentQualifiers>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>CF 500</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195203-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>195204</Austr>
				<PresentationName>C-Flox</PresentationName>
    			<PresentionStrength>750mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ciprofloxacin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>C-Flox</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ciprofloxacin</ActiveIngredient>
						<ReleaseDate>2022-08-08 13:27:55.0</ReleaseDate>
					</DocumentQualifiers>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>CF 750</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195204-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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			</Presentations>
		</Brand><Brand>
			<brandname>Cabaser</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>57360</Austr>
				<PresentationName>Cabaser</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Cabergoline</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cabaser</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>cabergoline</ActiveIngredient>
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				<Images>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>19/09/2011 16:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>7 01</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>57360-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>57367</Austr>
				<PresentationName>Cabaser</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Cabergoline</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cabaser</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>cabergoline</ActiveIngredient>
						<ReleaseDate>2019-10-14 09:48:12.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/09/2011 16:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>7 02</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>57367-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cadivast</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>199210</Austr>
				<PresentationName>Cadivast</PresentationName>
    			<PresentionStrength>5mg/80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Atorvastatin calcium,Amlodipine besilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cadivast</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amlodipine besilate with atorvastatin calcium</ActiveIngredient>
						<ReleaseDate>2021-05-31 06:57:42.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/09/2014 13:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>AA 7</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199210-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199213</Austr>
				<PresentationName>Cadivast</PresentationName>
    			<PresentionStrength>5mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Amlodipine besilate,Atorvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cadivast</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccadiv20521</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amlodipine besilate with atorvastatin calcium</ActiveIngredient>
						<ReleaseDate>2021-05-31 06:57:42.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/03/2018 12:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>AA 4</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199213-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199214</Austr>
				<PresentationName>Cadivast</PresentationName>
    			<PresentionStrength>5mg/40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Amlodipine besilate,Atorvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cadivast</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccadiv20521</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amlodipine besilate with atorvastatin calcium</ActiveIngredient>
						<ReleaseDate>2021-05-31 06:57:42.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/10/2016 14:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>AA 6</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199214-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199215</Austr>
				<PresentationName>Cadivast</PresentationName>
    			<PresentionStrength>10mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Atorvastatin calcium,Amlodipine besilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cadivast</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccadiv20521</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amlodipine besilate with atorvastatin calcium</ActiveIngredient>
						<ReleaseDate>2021-05-31 06:57:42.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/09/2014 13:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>barrel-shaped</Shape>
							<Side1Marking>AA 8</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199215-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199217</Austr>
				<PresentationName>Cadivast</PresentationName>
    			<PresentionStrength>10mg/80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Atorvastatin calcium,Amlodipine besilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cadivast</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccadiv20521</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amlodipine besilate with atorvastatin calcium</ActiveIngredient>
						<ReleaseDate>2021-05-31 06:57:42.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/09/2014 13:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>AA 11</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199217-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199222</Austr>
				<PresentationName>Cadivast</PresentationName>
    			<PresentionStrength>5mg/20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Atorvastatin calcium,Amlodipine besilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cadivast</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccadiv20521</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amlodipine besilate with atorvastatin calcium</ActiveIngredient>
						<ReleaseDate>2021-05-31 06:57:42.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/09/2014 13:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AA 5</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199222-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199223</Austr>
				<PresentationName>Cadivast</PresentationName>
    			<PresentionStrength>10mg/20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Amlodipine besilate,Atorvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cadivast</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amlodipine besilate with atorvastatin calcium</ActiveIngredient>
						<ReleaseDate>2021-05-31 06:57:42.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/03/2018 12:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>AA 9</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199223-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199225</Austr>
				<PresentationName>Cadivast</PresentationName>
    			<PresentionStrength>10mg/40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Amlodipine besilate,Atorvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cadivast</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccadiv20521</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amlodipine besilate with atorvastatin calcium</ActiveIngredient>
						<ReleaseDate>2021-05-31 06:57:42.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/10/2016 14:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AA 10</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199225-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Caduet</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>100695</Austr>
				<PresentationName>Caduet</PresentationName>
    			<PresentionStrength>5mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besylate,Atorvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/08/2008 13:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>CDT 051</Side1Marking>
							<Side2Marking>Pfizer</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>100695-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>100696</Austr>
				<PresentationName>Caduet</PresentationName>
    			<PresentionStrength>5mg/20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium,Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/08/2008 13:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>CDT 052</Side1Marking>
							<Side2Marking>Pfizer</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>100696-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>100697</Austr>
				<PresentationName>Caduet</PresentationName>
    			<PresentionStrength>5mg/40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium,Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>CDT 054</Side1Marking>
							<Side2Marking>Pfizer</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>100697-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>100698</Austr>
				<PresentationName>Caduet</PresentationName>
    			<PresentionStrength>5mg/80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium,Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/09/2011 16:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>CDT 058</Side1Marking>
							<Side2Marking>Pfizer</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>100698-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>100700</Austr>
				<PresentationName>Caduet</PresentationName>
    			<PresentionStrength>10mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besylate,Atorvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/09/2008 15:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>CDT 101</Side1Marking>
							<Side2Marking>Pfizer</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>100700-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>100701</Austr>
				<PresentationName>Caduet</PresentationName>
    			<PresentionStrength>10mg/20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besylate,Atorvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/09/2008 15:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>CDT 102</Side1Marking>
							<Side2Marking>Pfizer</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>100701-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>100702</Austr>
				<PresentationName>Caduet</PresentationName>
    			<PresentionStrength>10mg/40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besylate,Atorvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/09/2008 15:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>CDT 104</Side1Marking>
							<Side2Marking>Pfizer</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>100702-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>100703</Austr>
				<PresentationName>Caduet</PresentationName>
    			<PresentionStrength>10mg/80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besylate,Atorvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/09/2008 15:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>CDT 108</Side1Marking>
							<Side2Marking>Pfizer</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>100703-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cal Sup</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>161196</Austr>
				<PresentationName>Cal Sup Chocolate</PresentationName>
    			<PresentionStrength>650mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/07/2010 15:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>speckled brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CAL SUP 650</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>161196-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>161196-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>164955</Austr>
				<PresentationName>Cal Sup Chocolate + Vitamin D 500IU</PresentationName>
    			<PresentionStrength>650mg + 500IU</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/07/2010 15:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>speckled brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CAL SUP + D</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>164955-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>164955-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>59914</Austr>
				<PresentationName>Cal Sup</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/04/2009 12:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CAL-SUP 500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>59914-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>59914-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cal-Care</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>192527</Austr>
				<PresentationName>Cal-Care</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 15:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>CALCARE</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192527-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>200095</Austr>
				<PresentationName>Cal-Care Plus</PresentationName>
    			<PresentionStrength>600mg/10mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 15:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>CAL-D</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>200095-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Calci-Tab</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>165284</Austr>
				<PresentationName>Calci-Tab</PresentationName>
    			<PresentionStrength>1.5g</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/09/2013 14:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>165284-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Calcitriol (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>230366</Austr>
				<PresentationName>Calcitriol AN</PresentationName>
    			<PresentionStrength>0.25mcg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red</Colour>
							<Scoring></Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>230366-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Calcitriol (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>240872</Austr>
				<PresentationName>APO-Calcitriol</PresentationName>
    			<PresentionStrength>0.25mcg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Calcitriol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red</Colour>
							<Scoring></Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>240872-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Calcitriol (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>149504</Austr>
				<PresentationName>Calcitriol-GA</PresentationName>
    			<PresentionStrength>0.25mcg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 14:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red</Colour>
							<Scoring></Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>149504-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Calindamin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>214410</Austr>
				<PresentationName>Calindamin</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/04/2018 12:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>CLIN 150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214410-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Calitrol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>232770</Austr>
				<PresentationName>Calitrol</PresentationName>
    			<PresentionStrength>0.25mcg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/11/2019 15:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red</Colour>
							<Scoring></Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>232770-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Calquence</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>321419</Austr>
				<PresentationName>Calquence</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>acalabrutinib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Calquence</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apccalqu11119</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>acalabrutinib</ActiveIngredient>
						<ReleaseDate>2019-11-27 15:05:32.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>18/09/2020 13:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue and yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>ACA 100mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>321419-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Caltrate</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>79534</Austr>
				<PresentationName>Caltrate 600mg with Vitamin D Tablets</PresentationName>
    			<PresentionStrength>1.5g/5mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-25 00:00:00'}</WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/02/2010 14:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light peach</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>CALTRATE</Side1Marking>
							<Side2Marking>D 600</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>79534-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>79535</Austr>
				<PresentationName>Caltrate Plus Tablets</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-25 00:00:00'}</WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/02/2010 14:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dusty rose</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>CALTRATE</Side1Marking>
							<Side2Marking>+ 600</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>79535-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>80707</Austr>
				<PresentationName>Caltrate 600mg Tablets</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-25 00:00:00'}</WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/02/2010 14:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>CALTRATE</Side1Marking>
							<Side2Marking>C 600</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>80707-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>81700</Austr>
				<PresentationName>Caltrate 600mg Tablets</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/02/2010 14:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>CALTRATE</Side1Marking>
							<Side2Marking>C 600</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>81700-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Campral</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>68410</Austr>
				<PresentationName>Campral</PresentationName>
    			<PresentionStrength>333mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Acamprosate calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Campral</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccampr10318</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>acamprosate calcium</ActiveIngredient>
						<ReleaseDate>2018-03-07 07:19:53.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>333</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>68410-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Candesan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>195443</Austr>
				<PresentationName>Candesan</PresentationName>
    			<PresentionStrength>16mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/04/2018 12:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L293</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195443-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>195459</Austr>
				<PresentationName>Candesan</PresentationName>
    			<PresentionStrength>32mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/10/2018 16:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L294</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195459-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Candesan Combi</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>204577</Austr>
				<PresentationName>Candesan Combi</PresentationName>
    			<PresentionStrength>16mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/04/2018 12:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L3 02</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204577-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>204578</Austr>
				<PresentationName>Candesan Combi</PresentationName>
    			<PresentionStrength>32mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/04/2018 12:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L3 04</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204578-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>204579</Austr>
				<PresentationName>Candesan Combi</PresentationName>
    			<PresentionStrength>32mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/04/2018 15:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L3 04</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204579-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Candesartan (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>195452</Austr>
				<PresentationName>Candesartan-GA</PresentationName>
    			<PresentionStrength>32mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 10:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L294</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195452-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>195491</Austr>
				<PresentationName>Candesartan-GA</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 10:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>292</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195491-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>195506</Austr>
				<PresentationName>Candesartan-GA</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 10:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>291</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195506-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>195513</Austr>
				<PresentationName>Candesartan-GA</PresentationName>
    			<PresentionStrength>16mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 10:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L293</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195513-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Candesartan cilexetil (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>195453</Austr>
				<PresentationName>Candesartan AN</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
				<Austr>195466</Austr>
				<PresentationName>Candesartan AN</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink mottled</Colour>
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			<Presentations>
				<Austr>195486</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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			<Presentations>
				<Austr>195497</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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		</Brand><Brand>
			<brandname>Candesartan cilexetil (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>210529</Austr>
				<PresentationName>APO-Candesartan</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Candesartan cilexetil</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
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							<Views>
							<View>
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								<ImageFileName>210529-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>210530</Austr>
				<PresentationName>APO-Candesartan</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Candesartan cilexetil</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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							<DoseForm>Tablets</DoseForm>
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								<ImageFileName>210530-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>210531</Austr>
				<PresentationName>APO-Candesartan</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
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							<Views>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>210532</Austr>
				<PresentationName>APO-Candesartan</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
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							<Views>
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		</Brand><Brand>
			<brandname>Candesartan cilexetil (Blooms the Chemist)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>260093</Austr>
				<PresentationName>Blooms The Chemist Candesartan</PresentationName>
    			<PresentionStrength>32mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
				<Austr>260094</Austr>
				<PresentationName>Blooms The Chemist Candesartan </PresentationName>
    			<PresentionStrength>16mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
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			<Presentations>
				<Austr>260095</Austr>
				<PresentationName>Blooms The Chemist Candesartan </PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Candesartan cilexetil</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
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				<PresentationName>Blooms The Chemist Candesartan </PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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			<brandname>Candesartan cilexetil (Generic Health)</brandname>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
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				<PresentationName>Candesartan GH</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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			<Presentations>
				<Austr>195503</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<brandname>Candesartan cilexetil (Pharmacor)</brandname>
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			<Presentations>
				<Austr>195448</Austr>
				<PresentationName>Pharmacor Candesartan</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>291</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195448-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>195469</Austr>
				<PresentationName>Pharmacor Candesartan</PresentationName>
    			<PresentionStrength>32mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/07/2014 11:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L294</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195469-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>195496</Austr>
				<PresentationName>Pharmacor Candesartan</PresentationName>
    			<PresentionStrength>16mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/07/2014 11:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L293</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195496-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>195500</Austr>
				<PresentationName>Pharmacor Candesartan</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/10/2014 13:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>292</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195500-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Candesartan cilexetil (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>147493</Austr>
				<PresentationName>Candesartan Sandoz</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/04/2014 14:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>8</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>147493-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>147496</Austr>
				<PresentationName>Candesartan Sandoz</PresentationName>
    			<PresentionStrength>32mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/04/2014 14:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>32</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>147496-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>147497</Austr>
				<PresentationName>Candesartan Sandoz</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/04/2014 14:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>147497-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>147498</Austr>
				<PresentationName>Candesartan Sandoz</PresentationName>
    			<PresentionStrength>16mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/04/2014 14:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>16</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>147498-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Candesartan cilexetil with hydrochlorothiazide (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>204586</Austr>
				<PresentationName>Candesartan HCTZ AN</PresentationName>
    			<PresentionStrength>16mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/11/2017 16:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L3 02</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204586-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>204587</Austr>
				<PresentationName>Candesartan HCTZ AN</PresentationName>
    			<PresentionStrength>32mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/08/2017 09:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L3 04</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204587-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>204588</Austr>
				<PresentationName>Candesartan HCTZ AN</PresentationName>
    			<PresentionStrength>32mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/11/2017 16:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L3 04</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204588-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Candesartan cilexetil with hydrochlorothiazide (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>210565</Austr>
				<PresentationName>APO-Candesartan HCTZ</PresentationName>
    			<PresentionStrength>16/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L3 02</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>210565-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>210566</Austr>
				<PresentationName>APO-Candesartan HCTZ</PresentationName>
    			<PresentionStrength>32/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L3 04</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>210566-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>210567</Austr>
				<PresentationName>APO-Candesartan HCTZ</PresentationName>
    			<PresentionStrength>32/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Candesartan cilexetil,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L3 04</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>210567-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Candesartan cilexetil with hydrochlorothiazide (Blooms the Chemist)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>259998</Austr>
				<PresentationName>Blooms the Chemist Candesartan HCTZ</PresentationName>
    			<PresentionStrength>32/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/05/2017 11:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow mottled</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L3 04</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>259998-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>259999</Austr>
				<PresentationName>Blooms the Chemist Candesartan HCTZ</PresentationName>
    			<PresentionStrength>16/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/05/2017 11:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink mottled</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L3 02</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>259999-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>260000</Austr>
				<PresentationName>Blooms the Chemist Candesartan HCTZ</PresentationName>
    			<PresentionStrength>32/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Candesartan cilexetil,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/05/2017 11:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink mottled</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L3 04</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>260000-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Candesartan cilexetil with hydrochlorothiazide (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>204580</Austr>
				<PresentationName>Candesartan HCT GH 16/12.5</PresentationName>
    			<PresentionStrength>16mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 11:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L3 02</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204580-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>204581</Austr>
				<PresentationName>Candesartan HCT GH 32/12.5</PresentationName>
    			<PresentionStrength>32mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 11:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L3 04</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204581-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>204582</Austr>
				<PresentationName>Candesartan HCT GH 32/25</PresentationName>
    			<PresentionStrength>32mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 11:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L3 04</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204582-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Candesartan cilexetil with hydrochlorothiazide (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>157942</Austr>
				<PresentationName>Candesartan/HCT Sandoz</PresentationName>
    			<PresentionStrength>16mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/04/2014 14:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>apricot mottled</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157942-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>195278</Austr>
				<PresentationName>Candesartan/HCT Sandoz</PresentationName>
    			<PresentionStrength>32mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Candesartan cilexetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/04/2014 14:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish brown mottled</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>H 32</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195278-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>195279</Austr>
				<PresentationName>Candesartan/HCT Sandoz</PresentationName>
    			<PresentionStrength>32mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Candesartan cilexetil,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/04/2014 14:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light brown mottled</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>32</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195279-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Candesartan HCT (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>204568</Austr>
				<PresentationName>Pharmacor Candesartan HCT</PresentationName>
    			<PresentionStrength>16mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/07/2014 11:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L3 02</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204568-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>204569</Austr>
				<PresentationName>Pharmacor Candesartan HCT</PresentationName>
    			<PresentionStrength>32mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/07/2014 11:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L3 04</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204569-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>204570</Austr>
				<PresentationName>Pharmacor Candesartan HCT</PresentationName>
    			<PresentionStrength>32mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/07/2014 11:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L3 04</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204570-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Candesartan HCTZ (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>204583</Austr>
				<PresentationName>Candesartan HCTZ-GA</PresentationName>
    			<PresentionStrength>16mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 10:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L3 02</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204583-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>204584</Austr>
				<PresentationName>Candesartan HCTZ-GA</PresentationName>
    			<PresentionStrength>32mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 10:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L3 04</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204584-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Canesoral</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>131744</Austr>
				<PresentationName>Canesoral</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2009 15:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>G</Side1Marking>
							<Side2Marking>FC 150</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>131744-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Canesten</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>92390</Austr>
				<PresentationName>Canesten Once Pessary</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Pessary</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2009 15:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Pessary</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>pellet-shaped</Shape>
							<Side1Marking>MU</Side1Marking>
							<Side2Marking>BAYER</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>92390-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>92391</Austr>
				<PresentationName>Canesten 6 Day Pessary</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Pessary</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/02/2010 10:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Pessary</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>pellet-shaped</Shape>
							<Side1Marking>P3</Side1Marking>
							<Side2Marking>BAYER</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>92391-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Capecitabine (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>213033</Austr>
				<PresentationName>Capecitabine AN</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>213033-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>213037</Austr>
				<PresentationName>Capecitabine AN</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>213037-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Capecitabine (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>202738</Austr>
				<PresentationName>Capecitabine Apotex</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Capecitabine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/03/2015 16:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C500</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>202738-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Capecitabine (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>201797</Austr>
				<PresentationName>Capecitabine Sandoz</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Capecitabine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/04/2015 09:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>201797-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>201800</Austr>
				<PresentationName>Capecitabine Sandoz</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Capecitabine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/04/2015 09:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>201800-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Capoten</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>19247</Austr>
				<PresentationName>Capoten</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/03/2018 11:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>square</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>19247-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>19248</Austr>
				<PresentationName>Capoten</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/03/2018 11:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>19248-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Captopril (Douglas)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>77284</Austr>
				<PresentationName>Douglas Captopril</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 11:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>W 904</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>77284-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>77285</Austr>
				<PresentationName>Douglas Captopril</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 12:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>W 903</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>77285-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Captopril (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>61416</Austr>
				<PresentationName>Captopril Sandoz</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Captopril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>cloverleaf</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>61416-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>61419</Austr>
				<PresentationName>Captopril Sandoz</PresentationName>
    			<PresentionStrength>12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Captopril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>61419-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>61420</Austr>
				<PresentationName>Captopril Sandoz</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Captopril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>cloverleaf</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>61420-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Carafate</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>14930</Austr>
				<PresentationName>Carafate</PresentationName>
    			<PresentionStrength>1g</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/11/2008 14:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>CARAFATE</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>14930-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Carbamazepine (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>78211</Austr>
				<PresentationName>Carbamazepine Sandoz</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Carbamazepine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Carbamazepine Sandoz</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvccaror11119</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>carbamazepine</ActiveIngredient>
						<ReleaseDate>2019-12-09 15:43:29.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>GK</Side1Marking>
							<Side2Marking>CG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>78211-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>78217</Austr>
				<PresentationName>Carbamazepine Sandoz</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Carbamazepine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Carbamazepine Sandoz</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvccaror11119</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>carbamazepine</ActiveIngredient>
						<ReleaseDate>2019-12-09 15:43:29.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>BW</Side1Marking>
							<Side2Marking>GEIGY</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>78217-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cardasa</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>201525</Austr>
				<PresentationName>Cardasa</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cardasa</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccarda10313</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>aspirin</ActiveIngredient>
						<ReleaseDate>2013-03-21 16:51:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>heart shape</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>201525-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cardiprin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>15357</Austr>
				<PresentationName>Cardiprin</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/03/2011 12:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>15357-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cardizem</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>46818</Austr>
				<PresentationName>Cardizem CD</PresentationName>
    			<PresentionStrength>180mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Diltiazem hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cardizem CD and Cardizem</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swccardi10621</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>diltiazem hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-06-25 09:06:11.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/05/2021 08:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue and light turquoise</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>46818-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>46822</Austr>
				<PresentationName>Cardizem CD</PresentationName>
    			<PresentionStrength>240mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Diltiazem hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cardizem CD and Cardizem</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swccardi10621</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>diltiazem hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-06-25 09:06:11.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>dark blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>46822-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>73179</Austr>
				<PresentationName>Cardizem</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Diltiazem hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cardizem CD and Cardizem</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swccardi10621</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>diltiazem hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-06-25 09:06:11.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow, speckled</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>17 72</Side1Marking>
							<Side2Marking>MARION</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73179-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>75251</Austr>
				<PresentationName>Cardizem CD</PresentationName>
    			<PresentionStrength>360mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Diltiazem hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cardizem CD and Cardizem</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swccardi10621</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>diltiazem hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-06-25 09:06:11.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/06/2008 08:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and light blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75251-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cardol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>262936</Austr>
				<PresentationName>Cardol</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sotalol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cardol 80 mg</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccar8011120</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>sotalol hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-12-01 07:35:42.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>02/05/2019 08:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SOT</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>262936-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>43241</Austr>
				<PresentationName>Cardol</PresentationName>
    			<PresentionStrength>160mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Sotalol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cardol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccardo11120</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>sotalol hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-12-01 07:35:29.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SL 160</Side1Marking>
							<Side2Marking>&#945;</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>43241-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Carlevent</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>195192</Austr>
				<PresentationName>Carlevent</PresentationName>
    			<PresentionStrength>200/50/200</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/02/2021 13:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LEC</Side1Marking>
							<Side2Marking>200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195192-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>195194</Austr>
				<PresentationName>Carlevent</PresentationName>
    			<PresentionStrength>75/18.75/200 </PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/02/2021 13:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LEC</Side1Marking>
							<Side2Marking>75</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195194-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>195198</Austr>
				<PresentationName>Carlevent</PresentationName>
    			<PresentionStrength>50/12.5/200 </PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/02/2021 13:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LEC</Side1Marking>
							<Side2Marking>50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195198-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>195747</Austr>
				<PresentationName>Carlevent</PresentationName>
    			<PresentionStrength>100/25/200 </PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/02/2021 13:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LEC</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195747-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>195748</Austr>
				<PresentationName>Carlevent</PresentationName>
    			<PresentionStrength>125/31.25/200 </PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/02/2021 13:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LEC</Side1Marking>
							<Side2Marking>125</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195748-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>195749</Austr>
				<PresentationName>Carlevent</PresentationName>
    			<PresentionStrength>150/37.5/200 </PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/02/2021 13:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LEC</Side1Marking>
							<Side2Marking>150</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195749-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cartia</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>12976</Austr>
				<PresentationName>Cartia</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/03/2009 11:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>12976-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Carvedilol (Amneal)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>174785</Austr>
				<PresentationName>Carvedilol AN</PresentationName>
    			<PresentionStrength>6.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Carvedilol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/11/2017 16:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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                    	<Phase>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Carvedilol</TGAIngredient>
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							<DoseForm>Tablets</DoseForm>
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							<Side1Marking>F 58</Side1Marking>
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		</Brand><Brand>
			<brandname>Carvedilol (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>123823</Austr>
				<PresentationName>Apo-Carvedilol</PresentationName>
    			<PresentionStrength>3.125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Carvedilol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>P logo</Side1Marking>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>123825</Austr>
				<PresentationName>Apo-Carvedilol</PresentationName>
    			<PresentionStrength>3.125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Carvedilol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>P logo</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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			</Presentations>
			<Presentations>
				<Austr>123828</Austr>
				<PresentationName>Apo-Carvedilol</PresentationName>
    			<PresentionStrength>6.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Carvedilol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>6.25</Side1Marking>
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							<Views>
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			<Presentations>
				<Austr>123833</Austr>
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    			<PresentionStrength>6.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Carvedilol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>6.25</Side1Marking>
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							<Views>
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			<Presentations>
				<Austr>123836</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Carvedilol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>12.5</Side1Marking>
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			<Presentations>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
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							<Side1Marking>12.5</Side1Marking>
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			<Presentations>
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			<Presentations>
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    			<Container></Container>
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			<brandname>Carvedilol (Generic Health)</brandname>
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			<Presentations>
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			<Presentations>
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			<Presentations>
				<Austr>123838</Austr>
				<PresentationName>GenRx Carvedilol</PresentationName>
    			<PresentionStrength>12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Carvedilol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/08/2008 09:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>12.5</Side1Marking>
							<Side2Marking>P logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>123838-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>123842</Austr>
				<PresentationName>GenRx Carvedilol</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Carvedilol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/08/2008 09:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>25</Side1Marking>
							<Side2Marking>P logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>123842-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Carvedilol (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>104391</Austr>
				<PresentationName>Carvedilol Sandoz</PresentationName>
    			<PresentionStrength>6.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Carvedilol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>104391-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>104396</Austr>
				<PresentationName>Carvedilol Sandoz</PresentationName>
    			<PresentionStrength>12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Carvedilol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red-brown</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>104396-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>104399</Austr>
				<PresentationName>Carvedilol Sandoz</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Carvedilol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to almost white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>104399-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Carvedilol (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>133041</Austr>
				<PresentationName>Terry White Chemists Carvedilol</PresentationName>
    			<PresentionStrength>3.125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Carvedilol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/08/2008 09:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>P logo</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133041-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>133042</Austr>
				<PresentationName>Terry White Chemists Carvedilol</PresentationName>
    			<PresentionStrength>6.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Carvedilol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>13/08/2008 13:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>6.25</Side1Marking>
							<Side2Marking>P logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133042-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>133043</Austr>
				<PresentationName>Terry White Chemists Carvedilol</PresentationName>
    			<PresentionStrength>12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Carvedilol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/08/2008 09:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>12.5</Side1Marking>
							<Side2Marking>P logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133043-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>133044</Austr>
				<PresentationName>Terry White Chemists Carvedilol</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Carvedilol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/08/2008 09:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>25</Side1Marking>
							<Side2Marking>P logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133044-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Catapres</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>17921</Austr>
				<PresentationName>Catapres</PresentationName>
    			<PresentionStrength>100mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>clonidine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Catapres 100 Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ixccatal20121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clonidine hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-03-16 08:40:58.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/11/2010 10:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>01C 01C</Side1Marking>
							<Side2Marking>Boehringer Ingelheim Logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>17921-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>78376</Austr>
				<PresentationName>Catapres</PresentationName>
    			<PresentionStrength>150mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>clonidine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Catapres 150 Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ixccatat20121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clonidine hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-03-16 08:41:10.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/11/2010 10:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>15C 15C</Side1Marking>
							<Side2Marking>Boehringer Ingelheim Logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>78376-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cavstat</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>234485</Austr>
				<PresentationName>Cavstat</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cavstat</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccvsta11216</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>rosuvastatin sodium</ActiveIngredient>
						<ReleaseDate>2016-12-08 14:57:54.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/12/2018 14:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>R</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234485-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>234508</Austr>
				<PresentationName>Cavstat</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cavstat</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccvsta11216</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>rosuvastatin sodium</ActiveIngredient>
						<ReleaseDate>2016-12-08 14:57:54.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>02/05/2019 08:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>R</Side1Marking>
							<Side2Marking>40</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234508-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>234514</Austr>
				<PresentationName>Cavstat</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cavstat</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccvsta11216</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>rosuvastatin sodium</ActiveIngredient>
						<ReleaseDate>2016-12-08 14:57:54.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>02/05/2019 08:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>R</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234514-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>234543</Austr>
				<PresentationName>Cavstat</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Cavstat</DocumentName>
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								<Format>PDF</Format>
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			</Presentations>
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			<brandname>Ceclor</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>58264</Austr>
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    			<PresentionStrength>375mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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			<brandname>Cefaclor (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>76226</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
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					</Versions>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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							<Side1Marking>CEFACLOR-GA 375 mg</Side1Marking>
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							<Views>
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				</Images>
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   				<WithdrawalDate></WithdrawalDate>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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			<Presentations>
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			<Presentations>
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			<Presentations>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/12/2018 16:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue opaque and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>MYLAN CE 100</Side1Marking>
							<Side2Marking>MYLAN CE 100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>296389-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Celebrex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>67901</Austr>
				<PresentationName>Celebrex</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Celecoxib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Celebrex</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goccelec11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>celecoxib</ActiveIngredient>
						<ReleaseDate>2021-10-25 18:18:32.0</ReleaseDate>
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				</Documents>
				<Images>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>21/09/2011 13:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white with two blue bands</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>7767</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>67901-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>67902</Austr>
				<PresentationName>Celebrex</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Celecoxib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Celebrex</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goccelec11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>celecoxib</ActiveIngredient>
						<ReleaseDate>2021-10-25 18:18:32.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/08/2008 10:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white with two gold bands</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>7767</Side1Marking>
							<Side2Marking>200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>67902-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Celecoxib (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>206832</Austr>
				<PresentationName>Celecoxib AN</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white with two blue bands</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>206832-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>206844</Austr>
				<PresentationName>Celecoxib AN</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white with two gold bands</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>206844-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Celecoxib (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>212785</Austr>
				<PresentationName>Celecoxib Apotex</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>celecoxib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>31/03/2020 11:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white to off-white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>CC</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>212785-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>212787</Austr>
				<PresentationName>Celecoxib Apotex</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>celecoxib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>31/03/2020 13:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white to off-white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>CC</Side1Marking>
							<Side2Marking>200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>212787-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>226145</Austr>
				<PresentationName>APO-Celecoxib</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Celecoxib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white with two blue bands</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>226145-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>226146</Austr>
				<PresentationName>APO-Celecoxib</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Celecoxib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white with two gold bands</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>226146-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Celecoxib (Blooms the Chemist)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>212786</Austr>
				<PresentationName>Celecoxib BTC</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>celecoxib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/04/2020 09:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white to off-white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>CC</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>212786-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>212788</Austr>
				<PresentationName>Celecoxib BTC</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>celecoxib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/04/2020 09:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white to off-white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>CC</Side1Marking>
							<Side2Marking>200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>212788-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>226149</Austr>
				<PresentationName>Blooms the Chemist Celecoxib</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Celecoxib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/05/2017 11:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white with two blue bands</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>226149-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>226150</Austr>
				<PresentationName>Blooms the Chemist Celecoxib</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Celecoxib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/05/2017 11:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white with two gold bands</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>226150-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Celecoxib (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>226147</Austr>
				<PresentationName>Chemmart Celecoxib</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Celecoxib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>10/02/2016 10:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white with two blue bands</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>226148</Austr>
				<PresentationName>Chemmart Celecoxib</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Celecoxib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<DateEffective>10/02/2016 10:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white with two gold bands</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Celecoxib (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>196178</Austr>
				<PresentationName>Celecoxib GH</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<Shape></Shape>
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			<Presentations>
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							<Scoring></Scoring>
							<Shape></Shape>
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								<ViewLabel>C</ViewLabel>
								<ImageFileName>196188-C01-01-BL600.jpg</ImageFileName>
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							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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						<DateEffective>29/07/2016 09:40</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Colour>opaque orange and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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			</Presentations>
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			<Presentations>
				<Austr>226151</Austr>
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    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Celecoxib</TGAIngredient>
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						<DateEffective>10/02/2016 11:37</DateEffective>
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							<Shape></Shape>
							<Side1Marking></Side1Marking>
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					</Versions>
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			</Presentations>
			<Presentations>
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				<PresentationName>Terry White Chemists Celecoxib</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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							<Shape></Shape>
							<Side1Marking></Side1Marking>
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								<ViewLabel>C</ViewLabel>
								<ImageFileName>226152-C01-01-BL600.jpg</ImageFileName>
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			<brandname>Celexi</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>206828</Austr>
				<PresentationName>Celexi</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>11/04/2018 15:45</DateEffective>
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							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
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								<ViewLabel>C</ViewLabel>
								<ImageFileName>206828-C01-01-BL600.jpg</ImageFileName>
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			<Presentations>
				<Austr>206831</Austr>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Colour>opaque white with 2 gold bands</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>206831-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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			</Presentations>
		</Brand><Brand>
			<brandname>Celica</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>175481</Austr>
				<PresentationName>Celica</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>12/09/2011 09:20</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>06</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>175481-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>CellCept</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>67313</Austr>
				<PresentationName>CellCept</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mycophenolate mofetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>CellCept</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>mycophenolate mofetil</ActiveIngredient>
						<ReleaseDate>2021-12-06 10:41:51.0</ReleaseDate>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/09/2008 10:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue and brown</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>CellCept 250</Side1Marking>
							<Side2Marking>Roche</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>67313-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>82372</Austr>
				<PresentationName>CellCept</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mycophenolate mofetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>CellCept</DocumentName>
						<DocumentTypes>
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						<ActiveIngredient>mycophenolate mofetil</ActiveIngredient>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>01/09/2008 10:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>lavender</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>Cellcept 500</Side1Marking>
							<Side2Marking>Roche</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82372-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Celsentri</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>137329</Austr>
				<PresentationName>Celsentri</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Maraviroc</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<QualiferData></QualiferData>
						<DocumentName>Celsentri</DocumentName>
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						<ActiveIngredient>maraviroc</ActiveIngredient>
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						<DateEffective>20/03/2013 15:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MVC 150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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			<Presentations>
				<Austr>137331</Austr>
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    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Maraviroc</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Side1Marking>MVC 300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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								<ImageFileName>137331-C01-02-BL600.jpg</ImageFileName>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>75827</Austr>
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    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>12/02/2010 14:37</DateEffective>
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							<Side1Marking>EC 3</Side1Marking>
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							<Views>
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			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>127421</Austr>
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    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-25 00:00:00'}</WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>triangular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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							<View>
								<ViewLabel>B</ViewLabel>
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			<Presentations>
				<Austr>117597</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
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    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
							<Colour>grey</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>SELECT</Side1Marking>
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			<Presentations>
				<Austr>149055</Austr>
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    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-25 00:00:00'}</WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>12/02/2010 14:36</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
							<Colour>grey</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>SELECT</Side1Marking>
							<Side2Marking>W 2</Side2Marking>
							<Views>
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								<ImageFileName>149055-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Cepacol Antibacterial</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>52421</Austr>
				<PresentationName>Cepacol Antibacterial Honey &amp; Lemon</PresentationName>
    			<PresentionStrength>1.3mg/5mg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2009 15:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Lozenges</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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								<ImageFileName>52421-A01-01-BL600.jpg</ImageFileName>
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							<View>
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    							<ImageFileName>52421-B01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>76287</Austr>
				<PresentationName>Cepacol Antibacterial Orange</PresentationName>
    			<PresentionStrength>1.3mg/6mg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Lozenges</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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    							<ImageFileName>76287-B01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cepacol Cough</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>10102</Austr>
				<PresentationName>Cepacol Cough</PresentationName>
    			<PresentionStrength>1.3/1/5/5.2mg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Lozenges</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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								<ImageFileName>10102-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
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    							<ImageFileName>10102-B01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cepacol Plus</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10097</Austr>
				<PresentationName>Cepacol Plus Anaesthetic + Antibacterial</PresentationName>
    			<PresentionStrength>10mg/1.3mg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Lozenges</DoseForm>
							<Colour>green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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			</Presentations>
			<Presentations>
				<Austr>57471</Austr>
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    			<PresentionStrength>1.3mg/8.2mg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Colour>purple</Colour>
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							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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		</Brand><Brand>
			<brandname>Cephalex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>204534</Austr>
				<PresentationName>Cephalex</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
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                    	<Phase>
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							<DoseForm>Capsules</DoseForm>
							<Colour>light green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>CEP</Side1Marking>
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							<Views>
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			<Presentations>
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    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Capsules</DoseForm>
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							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>CEP</Side1Marking>
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							<Views>
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		</Brand><Brand>
			<brandname>Cephalexin (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>148200</Austr>
				<PresentationName>Cephalexin AN</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Capsules</DoseForm>
							<Colour>dark green and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
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							<Views>
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			</Presentations>
			<Presentations>
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				<PresentationName>Cephalexin AN</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient></TGAIngredient>
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							<Scoring></Scoring>
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							<Views>
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		</Brand><Brand>
			<brandname>Cephalexin (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>133852</Austr>
				<PresentationName>APO-Cephalexin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Cephalexin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>RX657</Side1Marking>
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							<Views>
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			</Presentations>
			<Presentations>
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				<PresentationName>APO-Cephalexin</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Cephalexin</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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                    	<Phase>
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							<Colour>dark green and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>RX656</Side1Marking>
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								<ViewLabel>C</ViewLabel>
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		</Brand><Brand>
			<brandname>Cephalexin (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>154381</Austr>
				<PresentationName>Cephalexin generichealth</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>dark green and light green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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		</Brand><Brand>
			<brandname>Cephalexin (Lupin)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>127390</Austr>
				<PresentationName>Cephalexin - Lupin</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>dark green and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
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							<Side2Marking>LUPIN</Side2Marking>
							<Views>
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								<ViewLabel>C</ViewLabel>
								<ImageFileName>127390-C01-01-BL600.jpg</ImageFileName>
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		</Brand><Brand>
			<brandname>Cephalexin (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>176784</Austr>
				<PresentationName>Pharmacor Cephalexin</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
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   				<WithdrawalDate></WithdrawalDate>
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							<PhaseItem>1</PhaseItem>
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								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>97506</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
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							<View>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<brandname>Cetirizine (Apohealth)</brandname>
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			<Presentations>
				<Austr>227636</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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		</Brand><Brand>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>composite pack</Container>
    			<TGAIngredient>Varenicline tartrate</TGAIngredient>
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   				<WithdrawalDate></WithdrawalDate>
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							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>71981-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cholecalciferol (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>218606</Austr>
				<PresentationName>Pharmacy Action Vitamin D</PresentationName>
    			<PresentionStrength>250mcg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>03/05/2017 14:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>translucent yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>218606-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cholstat</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>98486</Austr>
				<PresentationName>Cholstat</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pravastatin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cholstat</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>pravastatin sodium</ActiveIngredient>
						<ReleaseDate>2022-01-25 18:32:49.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PR 10</Side1Marking>
							<Side2Marking>G G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>98486-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>98488</Austr>
				<PresentationName>Cholstat</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pravastatin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cholstat</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcchols10122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>pravastatin sodium</ActiveIngredient>
						<ReleaseDate>2022-01-25 18:32:49.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PR 20</Side1Marking>
							<Side2Marking>G G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>98488-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>98489</Austr>
				<PresentationName>Cholstat</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pravastatin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cholstat</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcchols10122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>pravastatin sodium</ActiveIngredient>
						<ReleaseDate>2022-01-25 18:32:49.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PR 40</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>98489-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cholvastin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>140038</Austr>
				<PresentationName>Cholvastin</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 10:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark yellow to yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>P2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>140038-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>140042</Austr>
				<PresentationName>Cholvastin</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 10:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark yellow to yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>P3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>140042-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cialis</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>128496</Austr>
				<PresentationName>Cialis</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tadalafil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cialis</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>lycciali10221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tadalafil</ActiveIngredient>
						<ReleaseDate>2021-03-02 14:11:46.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>13/10/2008 10:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>almond-shaped</Shape>
							<Side1Marking>C5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>128496-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>81137</Austr>
				<PresentationName>Cialis</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tadalafil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cialis</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tadalafil</ActiveIngredient>
						<ReleaseDate>2021-03-02 14:11:46.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>13/10/2008 10:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>almond-shaped</Shape>
							<Side1Marking>C20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>81137-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>90590</Austr>
				<PresentationName>Cialis</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tadalafil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cialis</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tadalafil</ActiveIngredient>
						<ReleaseDate>2021-03-02 14:11:46.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>13/10/2008 10:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>almond-shaped</Shape>
							<Side1Marking>C10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>90590-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cidala</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>277540</Austr>
				<PresentationName>Cidala</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/07/2021 16:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow to light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L339</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>277540-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>277550</Austr>
				<PresentationName>Cidala</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/07/2021 16:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow to light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>338</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>277550-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>277558</Austr>
				<PresentationName>Cidala</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/07/2021 16:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow to light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>337</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>277558-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cifran</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>135660</Austr>
				<PresentationName>Cifran</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/02/2009 13:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>250</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135660-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>135661</Austr>
				<PresentationName>Cifran</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/02/2009 13:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>caplet-shaped</Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135661-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>135662</Austr>
				<PresentationName>Cifran</PresentationName>
    			<PresentionStrength>750mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/02/2009 13:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>caplet-shaped</Shape>
							<Side1Marking>750</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135662-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cilamox</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>286257</Austr>
				<PresentationName>Cilamox</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>amoxicillin trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cilamox</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goccilam10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amoxicillin sodium</ActiveIngredient>
						<ReleaseDate>2022-02-08 07:26:04.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/10/2022 14:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>286257-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>286258</Austr>
				<PresentationName>Cilamox</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>amoxicillin trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cilamox</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goccilam10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amoxicillin sodium</ActiveIngredient>
						<ReleaseDate>2022-02-08 07:26:04.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/10/2022 14:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>286258-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cilatil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>215923</Austr>
				<PresentationName>Cilatil</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>tadalafil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cilatil</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccilal10521</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tadalafil</ActiveIngredient>
						<ReleaseDate>2021-05-21 09:41:06.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/10/2022 13:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TL 2</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>215923-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>215926</Austr>
				<PresentationName>Cilatil</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>tadalafil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cilatil</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccilal10521</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tadalafil</ActiveIngredient>
						<ReleaseDate>2021-05-21 09:41:06.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/10/2022 13:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TL4</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>215926-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>215927</Austr>
				<PresentationName>Cilatil</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>tadalafil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cilatil</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccilal10521</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tadalafil</ActiveIngredient>
						<ReleaseDate>2021-05-21 09:41:06.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/10/2022 13:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TL3</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>215927-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cilex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>144109</Austr>
				<PresentationName>Cilex</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 12:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>dark green and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>250</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>144109-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>144110</Austr>
				<PresentationName>Cilex</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 12:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>dark green and light green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>144110-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cilicaine</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>339012</Austr>
				<PresentationName>Cilicaine VK</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>phenoxymethylpenicillin potassium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cilicaine VK</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goccilvk10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>phenoxymethylpenicillin potassium</ActiveIngredient>
						<ReleaseDate>2022-07-28 15:02:47.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>31/01/2022 16:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>maroon</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>339012-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>339013</Austr>
				<PresentationName>Cilicaine VK</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>phenoxymethylpenicillin potassium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cilicaine VK</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goccilvk10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>phenoxymethylpenicillin potassium</ActiveIngredient>
						<ReleaseDate>2022-07-28 15:02:47.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>31/01/2022 16:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>maroon</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>339013-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>55675</Austr>
				<PresentationName>Cilicaine VK</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>phenoxymethylpenicillin potassium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/03/2010 11:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque rusty red</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>55675-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cinacalcet hydrochloride (Viatris)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>289379</Austr>
				<PresentationName>Cinacalcet viatris</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>cinacalcet hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cinacalcet Viatris</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccinam11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>cinacalcet hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-10 08:46:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>31/01/2022 12:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>CI30</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>289379-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>289380</Austr>
				<PresentationName>Cinacalcet Viatris</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>cinacalcet hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cinacalcet Viatris</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>cinacalcet hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-10 08:46:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>31/01/2022 12:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>CI60</Side1Marking>
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			<Presentations>
				<Austr>289381</Austr>
				<PresentationName>Cinacalcet Viatris</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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							<DoseForm>Tablets</DoseForm>
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							<Shape>oval</Shape>
							<Side1Marking>CI90</Side1Marking>
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			<brandname>Cipramil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>61164</Austr>
				<PresentationName>Cipramil</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Citalopram hydrobromide</TGAIngredient>
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					<DocumentQualifiers>
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								<Format>PDF</Format>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
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			</Presentations>
		</Brand><Brand>
			<brandname>Ciprofloxacin (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>175436</Austr>
				<PresentationName>Ciprofloxacin AN</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>15/11/2017 16:24</DateEffective>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>F 22</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>175438</Austr>
				<PresentationName>Ciprofloxacin AN</PresentationName>
    			<PresentionStrength>750mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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						<DateEffective>15/11/2017 16:24</DateEffective>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>C</Side1Marking>
							<Side2Marking>93</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>175438-C01-01-BL600.jpg</ImageFileName>
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		</Brand><Brand>
			<brandname>Ciprofloxacin (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>135650</Austr>
				<PresentationName>APO-Ciprofloxacin </PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ciprofloxacin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>22/05/2016 20:56</DateEffective>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>250</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135650-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
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			</Presentations>
			<Presentations>
				<Austr>135651</Austr>
				<PresentationName>APO-Ciprofloxacin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ciprofloxacin hydrochloride</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135651-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>135652</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ciprofloxacin hydrochloride</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<VersionSequence>1</VersionSequence>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>750</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135652-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Ciprofloxacin (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>127781</Austr>
				<PresentationName>Ciprofloxacin-BW</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/09/2011 15:10</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to creamish white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>CPR 500</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127781-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>127782</Austr>
				<PresentationName>Ciprofloxacin-BW</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>04/12/2008 14:11</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white to creamish white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>CPR 750</Side1Marking>
							<Side2Marking>BL</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127782-C01-01-BL600.jpg</ImageFileName>
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				</Images>
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		</Brand><Brand>
			<brandname>Ciprofloxacin (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>132826</Austr>
				<PresentationName>Ciprofloxacin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to creamish white</Colour>
							<Scoring>scored</Scoring>
							<Shape>caplet</Shape>
							<Side1Marking>CPR 500</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>132830</Austr>
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    			<PresentionStrength>750mg</PresentionStrength>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
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							<Colour>white to creamish white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>caplet</Shape>
							<Side1Marking>CPR 750</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>132830-C01-01-BL600.jpg</ImageFileName>
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		</Brand><Brand>
			<brandname>Ciprofloxacin (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>81460</Austr>
				<PresentationName>Ciprofloxacin Sandoz</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ciprofloxacin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>cip 250</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>81461</Austr>
				<PresentationName>Ciprofloxacin Sandoz</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ciprofloxacin hydrochloride</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>cip 500</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>81462</Austr>
				<PresentationName>Ciprofloxacin Sandoz</PresentationName>
    			<PresentionStrength>750mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ciprofloxacin hydrochloride</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>cip 750</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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		</Brand><Brand>
			<brandname>Ciprol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>82475</Austr>
				<PresentationName>Ciprol</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
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			<Presentations>
				<Austr>82477</Austr>
				<PresentationName>Ciprol</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>07/11/2019 15:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>CR 500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82477-C01-02-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>82479</Austr>
				<PresentationName>Ciprol</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/11/2019 15:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CR 250</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82479-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ciproxin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>35317</Austr>
				<PresentationName>Ciproxin</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/04/2010 10:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CIP 250</Side1Marking>
							<Side2Marking>Bayer Cross</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>35317-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>35361</Austr>
				<PresentationName>Ciproxin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/04/2010 10:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>CIP 500</Side1Marking>
							<Side2Marking>BAYER</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>35361-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>35367</Austr>
				<PresentationName>Ciproxin</PresentationName>
    			<PresentionStrength>750mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/04/2010 10:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>CIP 750</Side1Marking>
							<Side2Marking>BAYER</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>35367-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Citalopram (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>158879</Austr>
				<PresentationName>Citalopram Amneal</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/08/2017 09:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158879-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>171336</Austr>
				<PresentationName>Citalopram AN</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Citalopram hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/07/2011 11:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>0 6</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>171336-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>171338</Austr>
				<PresentationName>Citalopram AN</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Citalopram hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/07/2011 11:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>0 7</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>171338-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Citalopram (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>150626</Austr>
				<PresentationName>Apo-Citalopram</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Citalopram hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2010 14:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>40</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>150626-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>150627</Austr>
				<PresentationName>Apo-Citalopram</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Citalopram hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2010 14:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>150627-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>226578</Austr>
				<PresentationName>APO-Citalopram </PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Citalopram hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking>BL</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>226578-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>226579</Austr>
				<PresentationName>APO-Citalopram </PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Citalopram hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>40</Side1Marking>
							<Side2Marking>BL</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>226579-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Citalopram (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>226580</Austr>
				<PresentationName>Chemmart Citalopram </PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Citalopram hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 21:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking>BL</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>226580-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Citalopram (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>158852</Austr>
				<PresentationName>Citalopram-GA</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 10:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>BL</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158852-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158916</Austr>
				<PresentationName>Citalopram-GA</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 10:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>BL</Side1Marking>
							<Side2Marking>40</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158916-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Citalopram (GenRx)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>101159</Austr>
				<PresentationName>GenRx Citalopram</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Citalopram hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/08/2008 08:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101159-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101225</Austr>
				<PresentationName>GenRx Citalopram</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Citalopram hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/08/2008 08:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>40</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101225-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Citalopram (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>101690</Austr>
				<PresentationName>Citalopram Sandoz</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Citalopram</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 11:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101690-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101691</Austr>
				<PresentationName>Citalopram Sandoz</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Citalopram</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 14:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101691-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>107061</Austr>
				<PresentationName>Citalopram Sandoz</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Citalopram</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 14:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C 40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>107061-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Citalopram (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>101222</Austr>
				<PresentationName>Terry White Chemists Citalopram</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Citalopram hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/08/2008 10:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101222-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>226581</Austr>
				<PresentationName>Terry White Chemists Citalopram </PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Citalopram hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 21:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking>BL</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>226581-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Citracal</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>129696</Austr>
				<PresentationName>Citracal + D</PresentationName>
    			<PresentionStrength>1.5g/12.5mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2009 15:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>CITRACAL</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>129696-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>131240</Austr>
				<PresentationName>Citracal</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2009 15:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>CITRACAL</Side1Marking>
							<Side2Marking>250</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>131240-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clarac</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>95756</Austr>
				<PresentationName>Clarac</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/07/2009 14:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>bright yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>CLA</Side1Marking>
							<Side2Marking>250</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>95756-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Claratyne</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>34698</Austr>
				<PresentationName>Claratyne</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/02/2011 13:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>(Logo) 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>34698-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Claratyne-D</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>53516</Austr>
				<PresentationName>Claratyne-D with Decongestant</PresentationName>
    			<PresentionStrength>5mg/120mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/06/2012 10:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>53516-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>53516-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clarithro</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>117197</Austr>
				<PresentationName>Clarithro</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>117197-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clarithromycin (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>184263</Austr>
				<PresentationName>Clarithromycin AN</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/11/2017 16:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>bright yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>CLA</Side1Marking>
							<Side2Marking>250</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184263-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clarithromycin (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>134850</Austr>
				<PresentationName>APO-Clarithromycin</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clarithromycin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/05/2010 10:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>CLA250</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>134850-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>134856</Austr>
				<PresentationName>APO-Clarithromycin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clarithromycin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/09/2017 09:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>CLA500</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>134856-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clarithromycin (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>101265</Austr>
				<PresentationName>Clarithromycin Sandoz</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clarithromycin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/09/2008 13:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101265-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clavam</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>202571</Austr>
				<PresentationName>Clavam</PresentationName>
    			<PresentionStrength>875mg/125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/07/2014 11:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>AM CL</Side1Marking>
							<Side2Marking>1000</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>202571-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cleocin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>134663</Austr>
				<PresentationName>Cleocin</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-03-28 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clindamycin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/09/2011 16:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Pfizer</Side1Marking>
							<Side2Marking>CLIN 150</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>134663-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clindamycin (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>214377</Austr>
				<PresentationName>APO-Clindamycin</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clindamycin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>CLIN 150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214377-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clindamycin (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>214365</Austr>
				<PresentationName>Chemmart Clindamycin</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clindamycin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/02/2016 10:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>CLIN 150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214365-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clindamycin (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>214411</Austr>
				<PresentationName>Terry White Chemists Clindamycin</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clindamycin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/02/2016 11:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>CLIN 150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214411-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clindamyk</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>214371</Austr>
				<PresentationName>Clindamyk</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clindamycin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Clindamyk</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcclinm10720</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clindamycin hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-07-15 08:06:27.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>02/05/2019 08:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>CLIN 150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214371-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clobemix</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>184084</Austr>
				<PresentationName>Clobemix</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/06/2020 11:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184084-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>184085</Austr>
				<PresentationName>Clobemix</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/02/2020 16:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to yellowish-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184085-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clofen</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>42146</Austr>
				<PresentationName>Clofen</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Baclofen</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Clofen</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcclofe10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>baclofen</ActiveIngredient>
						<ReleaseDate>2022-06-08 16:30:28.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>BN 10</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>42146-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>42147</Austr>
				<PresentationName>Clofen</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Baclofen</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Clofen</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcclofe10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>baclofen</ActiveIngredient>
						<ReleaseDate>2022-06-08 16:30:28.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>BN 25</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>42147-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clomid</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10103</Austr>
				<PresentationName>Clomid</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clomiphene citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/06/2008 10:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CLOMID 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10103-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clomipramine Hydrochloride (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>73878</Austr>
				<PresentationName>APO-Clomipramine</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clomipramine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/08/2008 09:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73878-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clomipramine Hydrochloride (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>73876</Austr>
				<PresentationName>Chemmart Clomipramine</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clomipramine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/08/2008 09:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73876-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clomipramine Hydrochloride (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>73875</Austr>
				<PresentationName>Terry White Chemists Clomipramine</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clomipramine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/08/2008 09:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73875-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clonac</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>145811</Austr>
				<PresentationName>Clonac</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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								<ImageFileName>265776-C01-01-BL600.jpg</ImageFileName>
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			<brandname>Clopidogrel (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>129642</Austr>
				<PresentationName>APO-Clopidogrel</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
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							<DoseForm>Tablets</DoseForm>
							<Colour>reddish-brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CL 75</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>129642-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
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			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
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			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
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							<Side1Marking>CL 75</Side1Marking>
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							<Views>
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			<brandname>Clopidogrel (Blooms the Chemist)</brandname>
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			<Presentations>
				<Austr>227622</Austr>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient>Clopidogrel hydrogen sulfate,Aspirin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>75-100</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>190326-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clopidogrel Aspirin (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>219057</Austr>
				<PresentationName>Clopidogrel Aspirin Sandoz</PresentationName>
    			<PresentionStrength>75mg/100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Aspirin,Clopidogrel hydrogen sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/03/2018 10:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>mottled purple</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>CL7</Side1Marking>
							<Side2Marking>S1</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>219057-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clopidogrel Aspirin (Winthrop)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>150470</Austr>
				<PresentationName>Clopidogrel Winthrop Plus Aspirin</PresentationName>
    			<PresentionStrength>75mg/100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Clopidogrel hydrogen sulfate,Aspirin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Clopidogrel Winthrop Plus Aspirin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcclopi10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clopidogrel with aspirin</ActiveIngredient>
						<ReleaseDate>2022-05-31 17:03:28.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/03/2012 11:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C75</Side1Marking>
							<Side2Marking>A100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>150470-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clopine</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>67947</Austr>
				<PresentationName>Clopine</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>clozapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Clopine</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfccloia10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clozapine</ActiveIngredient>
						<ReleaseDate>2022-03-02 10:41:08.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 16:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>67947-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>67948</Austr>
				<PresentationName>Clopine</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>clozapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Clopine</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfccloia10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clozapine</ActiveIngredient>
						<ReleaseDate>2022-03-02 10:41:08.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 16:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>67948-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>93972</Austr>
				<PresentationName>Clopine</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>clozapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Clopine</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfccloia10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clozapine</ActiveIngredient>
						<ReleaseDate>2022-03-02 10:41:08.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 16:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>93972-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>93973</Austr>
				<PresentationName>Clopine</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>clozapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Clopine</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfccloia10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clozapine</ActiveIngredient>
						<ReleaseDate>2022-03-02 10:41:08.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 16:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>93973-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>95557</Austr>
				<PresentationName>Clopine</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>clozapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Clopine</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfccloia10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clozapine</ActiveIngredient>
						<ReleaseDate>2022-03-02 10:41:08.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 16:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>95557-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>95559</Austr>
				<PresentationName>Clopine</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>clozapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Clopine</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfccloia10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clozapine</ActiveIngredient>
						<ReleaseDate>2022-03-02 10:41:08.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 16:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>95559-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>95560</Austr>
				<PresentationName>Clopine</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>clozapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Clopine</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfccloia10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clozapine</ActiveIngredient>
						<ReleaseDate>2022-03-02 10:41:08.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 16:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>95560-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>95561</Austr>
				<PresentationName>Clopine</PresentationName>
    			<PresentionStrength>200mg </PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>clozapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Clopine</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfccloia10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clozapine</ActiveIngredient>
						<ReleaseDate>2022-03-02 10:41:08.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 16:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>95561-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clopixol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>45077</Austr>
				<PresentationName>Clopixol</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Zuclopenthixol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Clopixol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>lucclopi10322</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>zuclopenthixol hydrochloride; zuclopenthixol acetate; zuclopenthixol decanoate</ActiveIngredient>
						<ReleaseDate>2022-03-28 12:00:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/09/2008 10:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light red brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>45077-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Clozaril</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>50510</Austr>
				<PresentationName>Clozaril</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clozapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Clozaril</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goccloza10322</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clozapine</ActiveIngredient>
						<ReleaseDate>2022-03-02 15:55:09.0</ReleaseDate>
					</DocumentQualifiers>
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   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient>Clozapine</TGAIngredient>
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						<QualiferData></QualiferData>
						<DocumentName>Clozaril</DocumentName>
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							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>CLOZ</Side1Marking>
							<Side2Marking>Z A</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>Superceded</VersionStatus>
						<DateEffective>19/11/2008 12:35</DateEffective>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ZA</Side1Marking>
							<Side2Marking>SANDOZ</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>50511-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>79930</Austr>
				<PresentationName>Clozaril</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Clozapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/11/2008 12:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ZA</Side1Marking>
							<Side2Marking>SANDOZ</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>79930-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>79932</Austr>
				<PresentationName>Clozaril</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Clozapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/11/2008 12:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>LO</Side1Marking>
							<Side2Marking>SANDOZ</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>79932-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Co-Diovan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>135782</Austr>
				<PresentationName>Co-Diovan</PresentationName>
    			<PresentionStrength>320/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Co-Diovan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>valsartan with hydrochlorothiazide</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/01/2011 13:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>HIL</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135782-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>135812</Austr>
				<PresentationName>Co-Diovan</PresentationName>
    			<PresentionStrength>320/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Co-Diovan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>valsartan with hydrochlorothiazide</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>CTI</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>96740</Austr>
				<PresentationName>Co-Diovan</PresentationName>
    			<PresentionStrength>80mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Co-Diovan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>valsartan with hydrochlorothiazide</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>HGH</Side1Marking>
							<Side2Marking>CG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>96741</Austr>
				<PresentationName>Co-Diovan</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Co-Diovan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>valsartan with hydrochlorothiazide</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/01/2009 10:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>HHH</Side1Marking>
							<Side2Marking>CG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>96742</Austr>
				<PresentationName>Co-Diovan</PresentationName>
    			<PresentionStrength>160mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Co-Diovan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/01/2009 10:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange-brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>HXH</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
		</Brand><Brand>
			<brandname>Cobasol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>170402</Austr>
				<PresentationName>Cobasol</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Cabergoline</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>7 01</Side1Marking>
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							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>170403</Austr>
				<PresentationName>Cobasol</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Cabergoline</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/02/2011 14:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
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							<Side1Marking>7 02</Side1Marking>
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							<Views>
							<View>
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		</Brand><Brand>
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			<Presentations>
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				<PresentationName>Codalgin</PresentationName>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>47807</Austr>
				<PresentationName>Codalgin Forte</PresentationName>
    			<PresentionStrength>500mg/30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-03-07 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>47807-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>71022</Austr>
				<PresentationName>Codalgin Plus</PresentationName>
    			<PresentionStrength>500mg/9.6mg/5.1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>71022-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Codapane Forte 500/30mg</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>285558</Austr>
				<PresentationName>Codapane Forte </PresentationName>
    			<PresentionStrength>500mg/30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>codeine phosphate hemihydrate,Paracetamol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Codapane Forte</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swccodap10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>paracetamol with codeine phosphate hemihydrate</ActiveIngredient>
						<ReleaseDate>2022-07-19 13:14:48.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/06/2021 14:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>P F</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>285558-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Codis</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>15358</Austr>
				<PresentationName>Codis</PresentationName>
    			<PresentionStrength>8/500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/03/2011 12:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>C-sword</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>15358-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>15358-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Codral</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>121310</Austr>
				<PresentationName>Codral Cold &amp; Flu + Cough Day &amp; Night</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/11/2016 10:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue-green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Day</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121310-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>reddish orange and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Night</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121310-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>51772</Austr>
				<PresentationName>Codral Original Day &amp; Night Cold &amp; Flu Tablets</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Codral Original Day &amp; Night</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pcccodnt30122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>codeine phosphate hemihydrate with paracetamol and pseudoephedrine hydrochloride and triprolidine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-05-11 09:32:11.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/11/2016 10:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>K7F</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>51772-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>51772-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>turquoise</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>S3F S3F</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>51772-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cold and Flu Fighter (Nyal)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>159099</Austr>
				<PresentationName>Nyal Cold and Flu Fighter</PresentationName>
    			<PresentionStrength>1.5g/1g/1g</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2010 16:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159099-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cold and Flu Fighter Day and Night (Nyal)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>158905</Austr>
				<PresentationName>Nyal Cold &amp; Flu Fighter Day &amp; Night</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2010 16:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158905-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158905-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Colese</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>316010</Austr>
				<PresentationName>Colese</PresentationName>
    			<PresentionStrength>135mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>mebeverine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Colese</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goccoles10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>mebeverine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-02-16 14:01:28.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/10/2022 14:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>316010-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>59746</Austr>
				<PresentationName>Colese</PresentationName>
    			<PresentionStrength>135mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>mebeverine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>MV 135</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>59746-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Colgout</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>27909</Austr>
				<PresentationName>Colgout</PresentationName>
    			<PresentionStrength>500mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Colchicine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/11/2008 14:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>27909-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Colofac</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>79335</Austr>
				<PresentationName>Colofac</PresentationName>
    			<PresentionStrength>135mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mebeverine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Colofac</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goccolof10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>mebeverine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-02-11 14:44:48.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/09/2008 15:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>79335-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Coloxyl with senna</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>59118</Austr>
				<PresentationName>Coloxyl with senna</PresentationName>
    			<PresentionStrength>50mg/8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/01/2013 14:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red-brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>59118-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Combivir</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>61489</Austr>
				<PresentationName>Combivir</PresentationName>
    			<PresentionStrength>150mg/300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Zidovudine,Lamivudine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Combivir</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>viccombi11121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lamivudine with zidovudine</ActiveIngredient>
						<ReleaseDate>2021-11-12 12:08:44.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 14:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>GX FC3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>61489-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Comfarol Forte</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>131137</Austr>
				<PresentationName>Comfarol Forte</PresentationName>
    			<PresentionStrength>500mg/30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Paracetamol,Codeine phosphate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Comfarol Forte</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swccomfa11221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>paracetamol with codeine phosphate hemihydrate</ActiveIngredient>
						<ReleaseDate>2021-12-09 09:10:41.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 16:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PF</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>131137-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Comtan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>68463</Austr>
				<PresentationName>Comtan</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Entacapone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/11/2008 12:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brownish-orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>COMTAN</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>68463-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Concerta</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>124502</Austr>
				<PresentationName>Concerta</PresentationName>
    			<PresentionStrength>27mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Concerta</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jccconce11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>methylphenidate hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-11-02 11:53:50.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/09/2008 15:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>grey</Colour>
							<Scoring></Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>alza 27</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>124502-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>93862</Austr>
				<PresentationName>Concerta</PresentationName>
    			<PresentionStrength>18mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Concerta</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jccconce11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>methylphenidate hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-11-02 11:53:50.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/09/2008 15:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring></Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>alza 18</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>93862-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>93863</Austr>
				<PresentationName>Concerta</PresentationName>
    			<PresentionStrength>36mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Concerta</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jccconce11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>methylphenidate hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-11-02 11:53:50.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/09/2008 15:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>alza 36</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>93863-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>93864</Austr>
				<PresentationName>Concerta</PresentationName>
    			<PresentionStrength>54mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Concerta</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jccconce11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>methylphenidate hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-11-02 11:53:50.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/09/2008 15:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brownish-red</Colour>
							<Scoring></Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>alza 54</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>93864-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Contrave</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>288372</Austr>
				<PresentationName>Contrave</PresentationName>
    			<PresentionStrength>8mg/90mg </PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>naltrexone hydrochloride,bupropion hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Contrave 8/90</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>iaccontv10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>naltrexone hydrochloride with bupropion hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-09-06 14:42:00.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/09/2019 16:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NB-890</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>288372-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>288372-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>CoPlavix</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>150443</Austr>
				<PresentationName>CoPlavix</PresentationName>
    			<PresentionStrength>75mg/100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Clopidogrel hydrogen sulfate,Aspirin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>CoPlavix</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swccopla10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clopidogrel with aspirin</ActiveIngredient>
						<ReleaseDate>2022-05-31 17:06:00.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2010 15:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C75</Side1Marking>
							<Side2Marking>A100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>150443-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Coralan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>107297</Austr>
				<PresentationName>Coralan</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ivabradine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Coralan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>seccoral10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ivabradine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-06-28 15:33:10.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/03/2009 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>salmon-pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>rod-shaped</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking>Servier logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>107297-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>107301</Austr>
				<PresentationName>Coralan</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ivabradine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Coralan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>seccoral10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ivabradine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-06-28 15:33:10.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/03/2009 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>salmon-pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>triangular</Shape>
							<Side1Marking>7.5</Side1Marking>
							<Side2Marking>Servier logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>107301-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cordarone X</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>15359</Austr>
				<PresentationName>Cordarone X</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amiodarone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cordarone X</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swccordx11121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amiodarone hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-12-01 14:21:50.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>100 logo</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>15359-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>15361</Austr>
				<PresentationName>Cordarone X</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amiodarone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cordarone X</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swccordx11121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amiodarone hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-12-01 14:21:50.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>200 logo</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>15361-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cordilox</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10681</Austr>
				<PresentationName>Cordilox SR</PresentationName>
    			<PresentionStrength>240mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Verapamil hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cordilox SR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goccordi10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>verapamil hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-05-11 16:07:25.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/10/2017 15:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light green</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>double Knoll triangle</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10681-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>54033</Austr>
				<PresentationName>Cordilox SR</PresentationName>
    			<PresentionStrength>180mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Verapamil hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cordilox SR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goccordi10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>verapamil hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-05-11 16:07:25.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/11/2008 08:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>SR 180</Side1Marking>
							<Side2Marking>KNOLL</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>54033-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cortate</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>27910</Austr>
				<PresentationName>Cortate</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Cortisone acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/11/2008 14:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>27910-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>27912</Austr>
				<PresentationName>Cortate</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Cortisone acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/11/2008 14:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>27912-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cortiment</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>225849</Austr>
				<PresentationName>Cortiment</PresentationName>
    			<PresentionStrength>9mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Budesonide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cortiment</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fpccortp10919</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>budesonide</ActiveIngredient>
						<ReleaseDate>2019-09-03 11:01:28.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/12/2016 16:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>MX9</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>225849-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cosamide</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>135207</Austr>
				<PresentationName>Cosamide</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bicalutamide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/09/2008 11:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>BIC 50</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135207-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>162829</Austr>
				<PresentationName>Cosamide 50</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bicalutamide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cosamide 50</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccosaf10920</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>bicalutamide</ActiveIngredient>
						<ReleaseDate>2020-09-23 07:38:20.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/12/2018 10:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>B 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>162829-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cosudex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>54639</Austr>
				<PresentationName>Cosudex</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bicalutamide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cosudex</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apccosud10517</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>bicalutamide</ActiveIngredient>
						<ReleaseDate>2017-05-26 17:19:04.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 10:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Cdx 50</Side1Marking>
							<Side2Marking>arrow shape</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>54639-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cough, Cold and Flu Dayand Night (Nyal)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>161723</Austr>
				<PresentationName>Nyal Cough, Cold &amp; Flu Day &amp; Night</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/04/2010 13:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>161723-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>purple</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>161723-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Coumadin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>14937</Austr>
				<PresentationName>Coumadin</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>warfarin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Coumadin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goccouma10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>warfarin sodium</ActiveIngredient>
						<ReleaseDate>2022-08-16 11:39:23.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/04/2012 14:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>lavender</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>COUMADIN 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>14937-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>42269</Austr>
				<PresentationName>Coumadin</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>warfarin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Coumadin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>warfarin sodium</ActiveIngredient>
						<ReleaseDate>2022-08-16 11:39:23.0</ReleaseDate>
					</DocumentQualifiers>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/04/2012 14:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light tan</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>COUMADIN 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>42279</Austr>
				<PresentationName>Coumadin</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>warfarin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
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							<AvailableFormats>
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							</AvailableFormats>
						</DocumentTypes>
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							</View>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Coveram</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>154438</Austr>
				<PresentationName>Coveram</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient>Perindopril arginine,Amlodipine besylate</TGAIngredient>
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				<Documents>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>perindopril arginine with amlodipine besilate</ActiveIngredient>
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						<DateEffective>02/03/2011 08:48</DateEffective>
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							<Side1Marking>5/5</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>154439</Austr>
				<PresentationName>Coveram</PresentationName>
    			<PresentionStrength>5mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Amlodipine besylate,Perindopril arginine</TGAIngredient>
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				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Coveram</DocumentName>
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							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>perindopril arginine with amlodipine besilate</ActiveIngredient>
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				</Documents>
				<Images>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>02/03/2011 08:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Shape>square</Shape>
							<Side1Marking>5/10</Side1Marking>
							<Side2Marking>Servier Logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154439-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>154440</Austr>
				<PresentationName>Coveram</PresentationName>
    			<PresentionStrength>10mg/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Amlodipine besylate,Perindopril arginine</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Coveram</DocumentName>
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							</AvailableFormats>
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						<DateEffective>02/03/2011 08:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>triangular</Shape>
							<Side1Marking>10/5</Side1Marking>
							<Side2Marking>Servier Logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154440-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>154441</Austr>
				<PresentationName>Coveram</PresentationName>
    			<PresentionStrength>10mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Perindopril arginine,Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Coveram</DocumentName>
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						<DateEffective>02/03/2011 08:50</DateEffective>
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							<Side1Marking>10/10</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154441-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Coversyl</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>101564</Austr>
				<PresentationName>Coversyl</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Perindopril arginine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Coversyl</DocumentName>
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							<AvailableFormats>
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					</DocumentQualifiers>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/03/2009 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101564-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101568</Austr>
				<PresentationName>Coversyl</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Perindopril arginine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Coversyl</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>perindopril arginine</ActiveIngredient>
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					</DocumentQualifiers>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/03/2009 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Side1Marking>Servier logo</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101569</Austr>
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    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Perindopril arginine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Coversyl</DocumentName>
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							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
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						<ActiveIngredient>perindopril arginine</ActiveIngredient>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>02/03/2009 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
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							<Side1Marking>heart</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101569-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Coversyl Plus</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>124552</Austr>
				<PresentationName>Coversyl Plus LD</PresentationName>
    			<PresentionStrength>2.5mg/0.625mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Perindopril arginine,Indapamide hemihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Coversyl Plus</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>perindopril arginine with indapamide hemihydrate</ActiveIngredient>
						<ReleaseDate>2022-07-20 16:30:43.0</ReleaseDate>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/03/2009 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>rod-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>124553</Austr>
				<PresentationName>Coversyl Plus</PresentationName>
    			<PresentionStrength>5mg/1.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Indapamide hemihydrate,Perindopril arginine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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							<AvailableFormats>
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						<DateEffective>02/03/2009 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
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							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>124553-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cozaar</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>54809</Austr>
				<PresentationName>Cozaar</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Losartan potassium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<QualiferData></QualiferData>
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						<DateEffective>26/09/2008 14:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<Views>
							<View>
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			</Presentations>
		</Brand><Brand>
			<brandname>Cozavan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>156234</Austr>
				<PresentationName>Cozavan</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient>Losartan potassium</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
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							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
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							<Side1Marking>A50</Side1Marking>
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							<View>
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			</Presentations>
			<Presentations>
				<Austr>156235</Austr>
				<PresentationName>Cozavan</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Losartan potassium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cozavan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccozan10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>losartan potassium</ActiveIngredient>
						<ReleaseDate>2022-07-26 14:13:24.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/03/2012 15:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156235-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Creon</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>158451</Austr>
				<PresentationName>Creon</PresentationName>
    			<PresentionStrength>40000u, 400mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Pancreatic extract</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Creon Capsules</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goccreca10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>pancreatic extract</ActiveIngredient>
						<ReleaseDate>2022-02-04 16:19:19.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/03/2011 20:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque brown/colourless-transparent</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158451-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158452</Austr>
				<PresentationName>Creon</PresentationName>
    			<PresentionStrength>25000u, 300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Pancreatic extract</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Creon Capsules</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goccreca10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>pancreatic extract</ActiveIngredient>
						<ReleaseDate>2022-02-04 16:19:19.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/03/2011 20:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light brown/colourless</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158452-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158453</Austr>
				<PresentationName>Creon</PresentationName>
    			<PresentionStrength>10000u, 150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Pancreatic extract</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Creon Capsules</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goccreca10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>pancreatic extract</ActiveIngredient>
						<ReleaseDate>2022-02-04 16:19:19.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/03/2011 20:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>dark brown/colourless</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158453-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>313833</Austr>
				<PresentationName>Creon</PresentationName>
    			<PresentionStrength>35000u, 420mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Pancreatic extract</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Creon Capsules</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goccreca10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>pancreatic extract</ActiveIngredient>
						<ReleaseDate>2022-02-04 16:19:19.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/10/2022 14:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red brown/colourless</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>313833-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cresemba</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>305452</Austr>
				<PresentationName>Cresemba</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>isavuconazonium sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cresemba</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfccrema10922</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>isavuconazole</ActiveIngredient>
						<ReleaseDate>2022-10-10 11:59:28.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>18/11/2021 10:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and reddish-brown</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>C</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>305452-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Crestor</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>119120</Austr>
				<PresentationName>Crestor</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Crestor</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fkccrest10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>rosuvastatin calcium</ActiveIngredient>
						<ReleaseDate>2022-08-30 13:46:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 11:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ZD4522 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>119120-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>119128</Austr>
				<PresentationName>Crestor</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Crestor</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fkccrest10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>rosuvastatin calcium</ActiveIngredient>
						<ReleaseDate>2022-08-30 13:46:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 11:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ZD4522 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>119128-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>119130</Austr>
				<PresentationName>Crestor</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Crestor</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fkccrest10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>rosuvastatin calcium</ActiveIngredient>
						<ReleaseDate>2022-08-30 13:46:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 11:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ZD4522 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>119130-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>119135</Austr>
				<PresentationName>Crestor</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Crestor</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fkccrest10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>rosuvastatin calcium</ActiveIngredient>
						<ReleaseDate>2022-08-30 13:46:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 11:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>ZD4522</Side1Marking>
							<Side2Marking>40</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>119135-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Crosuva</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>183737</Austr>
				<PresentationName>Crosuva</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/07/2019 16:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROS 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183737-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183739</Austr>
				<PresentationName>Crosuva</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/06/2019 16:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROS 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183739-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183741</Austr>
				<PresentationName>Crosuva</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/06/2019 16:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROS 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183741-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183743</Austr>
				<PresentationName>Crosuva</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/06/2019 16:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>ROS</Side1Marking>
							<Side2Marking>40</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183743-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Crysanal</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>67927</Austr>
				<PresentationName>Crysanal</PresentationName>
    			<PresentionStrength>550mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Naproxen sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Crysanal</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>iyccrysa10921</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>naproxen sodium</ActiveIngredient>
						<ReleaseDate>2021-10-07 16:11:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/09/2008 10:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>NPS 550</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>67927-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Curam</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>198108</Austr>
				<PresentationName>Curam Duo</PresentationName>
    			<PresentionStrength>500mg/125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>amoxicillin trihydrate,Potassium clavulanate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>198108-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>198109</Austr>
				<PresentationName>Curam Duo Forte</PresentationName>
    			<PresentionStrength>875mg/125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>amoxicillin trihydrate,Potassium clavulanate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>198109-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>82829</Austr>
				<PresentationName>Curam Duo Forte</PresentationName>
    			<PresentionStrength>875mg/125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient>amoxicillin trihydrate,Potassium clavulanate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/09/2008 17:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82829-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>82830</Austr>
				<PresentationName>Curam Duo</PresentationName>
    			<PresentionStrength>500mg/125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient>amoxicillin trihydrate,Potassium clavulanate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/09/2008 17:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82830-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cycloblastin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>73468</Austr>
				<PresentationName>Cycloblastin</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Cyclophosphamide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/09/2011 16:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73468-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cyclosporin (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>186358</Austr>
				<PresentationName>Cyclosporin Sandoz</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Cyclosporin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cyclosporin Sandoz</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvccicor11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ciclosporin</ActiveIngredient>
						<ReleaseDate>2022-10-25 09:27:14.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue-grey</Colour>
							<Scoring></Scoring>
							<Shape>oval</Shape>
							<Side1Marking>NVR 25mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>186358-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>186359</Austr>
				<PresentationName>Cyclosporin Sandoz</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Cyclosporin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cyclosporin Sandoz</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvccicor11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ciclosporin</ActiveIngredient>
						<ReleaseDate>2022-10-25 09:27:14.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow-white</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>NVR 50mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>186359-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>186361</Austr>
				<PresentationName>Cyclosporin Sandoz</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Cyclosporin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cyclosporin Sandoz</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvccicor11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ciclosporin</ActiveIngredient>
						<ReleaseDate>2022-10-25 09:27:14.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue-grey</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>NVR 100mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>186361-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cyklokapron</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>14463</Austr>
				<PresentationName>Cyklokapron</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Tranexamic acid</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cyklokapron</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfccyklt10420</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tranexamic acid</ActiveIngredient>
						<ReleaseDate>2020-05-21 14:13:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/09/2011 16:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>CY</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>14463-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cymbalta</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>120382</Austr>
				<PresentationName>Cymbalta</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Duloxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cymbalta</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>lyccymbt11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>duloxetine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-19 18:06:27.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/02/2009 09:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque blue and opaque white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>9543</Side1Marking>
							<Side2Marking>30mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>120382-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>120389</Austr>
				<PresentationName>Cymbalta</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Duloxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cymbalta</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>lyccymbt11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>duloxetine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-19 18:06:27.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/02/2009 09:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque blue and opaque green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>9542</Side1Marking>
							<Side2Marking>60mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>120389-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cyprone</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>266552</Austr>
				<PresentationName>Cyprone</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>cyproterone acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cyprone 50</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccypr510920</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>cyproterone acetate</ActiveIngredient>
						<ReleaseDate>2020-09-07 08:41:56.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/12/2018 10:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>266552-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>266553</Austr>
				<PresentationName>Cyprone</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>cyproterone acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cyprone 100</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccyp1010920</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>cyproterone acetate</ActiveIngredient>
						<ReleaseDate>2020-09-07 08:41:50.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>02/05/2019 08:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>CPA 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>266553-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cyprostat</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>156921</Austr>
				<PresentationName>Cyprostat</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/09/2014 13:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>BV hexagon</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156921-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>51450</Austr>
				<PresentationName>Cyprostat</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2010 09:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>LA LA</Side1Marking>
							<Side2Marking>hexagon</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>51450-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>76119</Austr>
				<PresentationName>Cyprostat</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2010 09:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>BV hexagon</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>76119-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cyproterone Acetate (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>184226</Austr>
				<PresentationName>Cyproterone AN</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/11/2017 16:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184226-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>184233</Austr>
				<PresentationName>Cyproterone AN</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/11/2017 16:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184233-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cyproterone Acetate (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>101534</Austr>
				<PresentationName>APO-Cyproterone</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>cyproterone acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/08/2008 11:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101534-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101535</Austr>
				<PresentationName>APO-Cyproterone </PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>cyproterone acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/08/2008 11:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101535-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cyproterone Acetate (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>107330</Austr>
				<PresentationName>Cyproterone Sandoz</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Cyproterone acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>107330-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>107331</Austr>
				<PresentationName>Cyproterone Sandoz</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Cyproterone acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>107331-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cystagon</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>60451</Austr>
				<PresentationName>Cystagon</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Cysteamine bitartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cystagon</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccysta10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>mercaptamine (cysteamine) bitartrate</ActiveIngredient>
						<ReleaseDate>2022-06-08 15:42:38.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/08/2008 09:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>MYLAN</Side1Marking>
							<Side2Marking>CYSTA 50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>60451-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>60452</Austr>
				<PresentationName>Cystagon</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Cysteamine bitartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cystagon</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afccysta10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>mercaptamine (cysteamine) bitartrate</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/08/2008 09:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>MYLAN</Side1Marking>
							<Side2Marking>CYSTAGON 150</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>60452-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Cytotec</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>63983</Austr>
				<PresentationName>Cytotec</PresentationName>
    			<PresentionStrength>200mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Misoprostol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Cytotec</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>misoprostol</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/09/2011 16:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>hexagonal</Shape>
							<Side1Marking>SEARLE 1461</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>63983-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>D-Penamine</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>14625</Austr>
				<PresentationName>D-Penamine</PresentationName>
    			<PresentionStrength>125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Penicillamine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>D-Penamine</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcd-pen10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>penicillamine</ActiveIngredient>
						<ReleaseDate>2022-07-05 12:25:17.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DS</Side1Marking>
							<Side2Marking>125</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>14625-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>14626</Austr>
				<PresentationName>D-Penamine</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Penicillamine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>D-Penamine</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcd-pen10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>penicillamine</ActiveIngredient>
						<ReleaseDate>2022-07-05 12:25:17.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DM</Side1Marking>
							<Side2Marking>250</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>14626-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dalacin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>12275</Austr>
				<PresentationName>Dalacin C</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clindamycin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dalacin C Capsules</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcdalcc10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clindamycin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-02-09 12:28:18.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/09/2011 16:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Pfizer</Side1Marking>
							<Side2Marking>CLIN 150</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>12275-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dantrium</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>42975</Austr>
				<PresentationName>Dantrium Capsules</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Dantrolene sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dantrium Capsules</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcdantc10920</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>dantrolene sodium hemiheptahydrate</ActiveIngredient>
						<ReleaseDate>2020-09-17 15:05:14.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/08/2008 13:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange and tan</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>DANTRIUM 25 mg</Side1Marking>
							<Side2Marking>0149 0030</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>42975-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>42976</Austr>
				<PresentationName>Dantrium Capsules</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Dantrolene sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dantrium Capsules</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcdantc10920</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>dantrolene sodium hemiheptahydrate</ActiveIngredient>
						<ReleaseDate>2020-09-17 15:05:14.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/08/2008 13:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange and tan</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>DANTRIUM 50 mg</Side1Marking>
							<Side2Marking>0149 0031</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>42976-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Daonil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>73683</Austr>
				<PresentationName>Daonil</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Glibenclamide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Daonil</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcdaoni10916</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>glibenclamide</ActiveIngredient>
						<ReleaseDate>2016-09-01 15:39:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>biplane oblong</Shape>
							<Side1Marking>LDI LDI</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73683-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dapa-Tabs</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>62367</Austr>
				<PresentationName>Dapa-Tabs</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Indapamide hemihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dapa-Tabs</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdapat10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>indapamide hemihydrate</ActiveIngredient>
						<ReleaseDate>2022-05-11 16:06:02.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>IE 2.5</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62367-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dapsone (Link Medical Products)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>104482</Austr>
				<PresentationName>Dapsone</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>17/08/2010 10:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>25 102</Side1Marking>
							<Side2Marking>JACOBUS</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>104482-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>104483</Austr>
				<PresentationName>Dapsone</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>17/08/2010 10:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>100 101</Side1Marking>
							<Side2Marking>JACOBUS</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>104483-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Daraprim</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>97456</Austr>
				<PresentationName>Daraprim</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Pyrimethamine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/03/2011 04:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>GS A3A</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>97456-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dasatinib (TE)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>332642</Austr>
				<PresentationName>TE-Dasatinib </PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablet</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>dasatinib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>TE-Dasatinib</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbctdasa11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>dasatinib</ActiveIngredient>
						<ReleaseDate>2021-10-25 11:47:46.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>332642-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>332645</Austr>
				<PresentationName>TE-Dasatinib</PresentationName>
    			<PresentionStrength>70mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>dasatinib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>TE-Dasatinib</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbctdasa11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>dasatinib</ActiveIngredient>
						<ReleaseDate>2021-10-25 11:47:46.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>70</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>332645-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>332649</Austr>
				<PresentationName>TE-Dasatinib</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>dasatinib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>TE-Dasatinib</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbctdasa11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>dasatinib</ActiveIngredient>
						<ReleaseDate>2021-10-25 11:47:46.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>332649-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>332656</Austr>
				<PresentationName>TE-Dasatinib </PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablet</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>dasatinib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>TE-Dasatinib</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbctdasa11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>dasatinib</ActiveIngredient>
						<ReleaseDate>2021-10-25 11:47:46.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>332656-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dasatinib (Teva)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>332651</Austr>
				<PresentationName>Dasatinib-Teva</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>dasatinib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dasatinib-Teva</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcdasat11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>dasatinib</ActiveIngredient>
						<ReleaseDate>2021-10-25 11:47:33.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/09/2022 11:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>332651-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>332652</Austr>
				<PresentationName>Dasatinib-Teva</PresentationName>
    			<PresentionStrength>70mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>dasatinib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dasatinib-Teva</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcdasat11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>dasatinib</ActiveIngredient>
						<ReleaseDate>2021-10-25 11:47:33.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/09/2022 11:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>70</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>332652-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>332653</Austr>
				<PresentationName>Dasatinib-Teva</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>dasatinib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dasatinib-Teva</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcdasat11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>dasatinib</ActiveIngredient>
						<ReleaseDate>2021-10-25 11:47:33.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/09/2022 11:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>332653-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>332654</Austr>
				<PresentationName>Dasatinib-Teva</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>dasatinib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dasatinib-Teva</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcdasat11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>dasatinib</ActiveIngredient>
						<ReleaseDate>2021-10-25 11:47:33.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/09/2022 11:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>332654-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>De-Gas</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10395</Austr>
				<PresentationName>De-Gas Capsules</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/02/2010 14:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>ivory</Colour>
							<Scoring></Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10395-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>59916</Austr>
				<PresentationName>De-Gas Extra Chewable Tablets</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-25 00:00:00'}</WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/02/2010 14:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>59916-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>59916-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Deferasirox (Teva)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>350822</Austr>
				<PresentationName>Deferasirox-Teva</PresentationName>
    			<PresentionStrength>360mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>deferasirox</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Deferasirox-Teva</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcdefer11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>deferasirox</ActiveIngredient>
						<ReleaseDate>2021-10-13 17:01:04.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/09/2022 11:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>ovaloid</Shape>
							<Side1Marking>360</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>350822-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>350824</Austr>
				<PresentationName>Deferasirox-Teva</PresentationName>
    			<PresentionStrength>180mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>deferasirox</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Deferasirox-Teva</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcdefer11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>deferasirox</ActiveIngredient>
						<ReleaseDate>2021-10-13 17:01:04.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/09/2022 11:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>medium blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>ovaloid</Shape>
							<Side1Marking>180</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>350824-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>350825</Austr>
				<PresentationName>Deferasirox-Teva</PresentationName>
    			<PresentionStrength>90mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>deferasirox</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Deferasirox-Teva</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcdefer11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>deferasirox</ActiveIngredient>
						<ReleaseDate>2021-10-13 17:01:04.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/09/2022 11:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>ovaloid</Shape>
							<Side1Marking>90</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>350825-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Demazin</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>97031</Austr>
				<PresentationName>Demazin Cough, Cold &amp; Flu Tablets</PresentationName>
    			<PresentionStrength>500/30/15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/10/2010 15:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>97031-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>97031-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>97036</Austr>
				<PresentationName>Demazin Cold &amp; Flu Tablets</PresentationName>
    			<PresentionStrength>500/30/2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/10/2010 15:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>97036-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>97036-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Demazin 6 Hour</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>18815</Austr>
				<PresentationName>Demazin 6 Hour Relief Tablets</PresentationName>
    			<PresentionStrength>60mg/4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/10/2010 11:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>(Logo)</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>18815-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Demazin Day &amp; Night</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>133205</Austr>
				<PresentationName>Demazin Day &amp; Night Cold &amp; Flu</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>CF SH</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133205-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>SH</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133205-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Demazin PE</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>152023</Austr>
				<PresentationName>Demazin PE Cold &amp; Flu Day &amp; Night Relief</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>14/10/2010 11:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>152023-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>152023-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152023-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>152024</Austr>
				<PresentationName>Demazin PE Cold &amp; Flu Relief</PresentationName>
    			<PresentionStrength>500/9/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/10/2010 11:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>152024-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>152024-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Deptran</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>17637</Austr>
				<PresentationName>Deptran</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Doxepin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Deptran</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>doxepin hydrochloride</ActiveIngredient>
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				<Images>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>violet</Colour>
							<Scoring>unscored</Scoring>
							<Shape>six-sided</Shape>
							<Side1Marking>DN 50</Side1Marking>
							<Side2Marking>&#945;</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>17637-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>308999</Austr>
				<PresentationName>Deptran</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>doxepin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Deptran</DocumentName>
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								<Format>PDF</Format>
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						<ActiveIngredient>doxepin hydrochloride</ActiveIngredient>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>DP 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>308999-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>60447</Austr>
				<PresentationName>Deptran</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Doxepin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>60447-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>60448</Austr>
				<PresentationName>Deptran</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Doxepin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Deptran</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>doxepin hydrochloride</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>60448-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Deralin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>17612</Austr>
				<PresentationName>Deralin</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Propranolol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Deralin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>propranolol hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-10-08 07:40:07.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PP 10</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>17612-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>17613</Austr>
				<PresentationName>Deralin</PresentationName>
    			<PresentionStrength>160mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Propranolol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Deralin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcderal11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>propranolol hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-10-08 07:40:07.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PP 160</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>17613-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>17614</Austr>
				<PresentationName>Deralin</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Propranolol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Deralin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcderal11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>propranolol hydrochloride</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PP 40</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>17614-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Deseril</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>62664</Austr>
				<PresentationName>Deseril</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>19/11/2008 12:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DSL</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62664-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Desfax</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>218061</Austr>
				<PresentationName>Desfax</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Desfax</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
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						</DocumentTypes>
						<ActiveIngredient>desvenlafaxine</ActiveIngredient>
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				<Images>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
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							<Side1Marking>L190</Side1Marking>
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			<Presentations>
				<Austr>218075</Austr>
				<PresentationName>Desfax</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Desloratadine (Apohealth)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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							<DoseForm>Tablets</DoseForm>
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							<Side1Marking>DL5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>202824-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Desven</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>218074</Austr>
				<PresentationName>Desven</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>diamond-shaped</Shape>
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							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>218074-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>218076</Austr>
				<PresentationName>Desven</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark brown to red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>diamond-shaped</Shape>
							<Side1Marking>L190</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>218076-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Desvenlafaxine (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>218082</Austr>
				<PresentationName>Desvenlafaxine Sandoz</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/10/2017 15:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark brown to red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>diamond-shaped</Shape>
							<Side1Marking>L190</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>218082-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>218083</Austr>
				<PresentationName>Desvenlafaxine Sandoz</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/10/2017 15:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>diamond-shaped</Shape>
							<Side1Marking>L189</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>218083-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Desvenlafaxine benzoate (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>218307</Austr>
				<PresentationName>APO-Desvenlafaxine MR</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>desvenlafaxine benzoate</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/12/2016 19:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DV</Side1Marking>
							<Side2Marking>50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>218307-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>227802</Austr>
				<PresentationName>APO-Desvenlafaxine MR</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>desvenlafaxine benzoate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/12/2016 19:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish-orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DV</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>227802-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Desvenlafaxine benzoate (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>227805</Austr>
				<PresentationName>Desvenlafaxine GH XR</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DV</Side1Marking>
							<Side2Marking>50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>227805-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>227806</Austr>
				<PresentationName>Desvenlafaxine GH XR</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish-orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DV</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>227806-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Detrusitol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>99393</Austr>
				<PresentationName>Detrusitol</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tolterodine tartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Detrusitol</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
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						<ActiveIngredient>tolterodine tartrate</ActiveIngredient>
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				<Images>
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						<DateEffective>22/09/2011 10:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>| TO |</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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								<ImageFileName>99393-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
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			</Presentations>
			<Presentations>
				<Austr>99394</Austr>
				<PresentationName>Detrusitol</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tolterodine tartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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								<Format>PDF</Format>
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						<ActiveIngredient>tolterodine tartrate</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/09/2008 13:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>| DT |</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>99394-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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		</Brand><Brand>
			<brandname>Dexamphetamine Sulfate (Aspen)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>19684</Austr>
				<PresentationName>Aspen Dexamphetamine</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/04/2012 14:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>D 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>19684-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dexmethsone</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>27915</Austr>
				<PresentationName>Dexmethsone</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Dexamethasone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/11/2008 14:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DS 4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>27915-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>27917</Austr>
				<PresentationName>Dexmethsone</PresentationName>
    			<PresentionStrength>500mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Dexamethasone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DS 0.5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>27917-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Diabex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>153699</Austr>
				<PresentationName>Diabex XR 500 and 1000</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Diabex XR 500 and 1000</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdiaxn11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-17 15:19:30.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/12/2018 10:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153699-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>40806</Austr>
				<PresentationName>Diabex</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Diabex</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdiabe11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-14 09:38:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/07/2012 16:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>DIABEX</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>40806-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>57645</Austr>
				<PresentationName>Diabex</PresentationName>
    			<PresentionStrength>850mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Diabex</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdiabe11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-14 09:38:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/07/2012 16:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>57645-A01-02-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>57645-B01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>81602</Austr>
				<PresentationName>Diabex</PresentationName>
    			<PresentionStrength>1g</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Diabex</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdiabe11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-14 09:38:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/04/2012 09:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>10 00</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>81602-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>98982</Austr>
				<PresentationName>Diabex XR</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>98982-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Diaformin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>120868</Austr>
				<PresentationName>Diaformin XR</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Diaformin XR (new formulation)</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdiaxr11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-17 15:25:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/07/2009 11:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>120868-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>208441</Austr>
				<PresentationName>Diaformin XR</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Diaformin XR (new formulation)</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdiaxr11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-17 15:25:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2019 10:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>208441-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>294057</Austr>
				<PresentationName>Diaformin</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Diaformin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdiafo10922</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-06 15:27:04.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/11/2022 12:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MF 3</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>294057-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>299825</Austr>
				<PresentationName>Diaformin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tables</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Diaformin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdiafo10922</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-06 15:27:04.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/11/2022 12:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>MF 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>299825-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>73806</Austr>
				<PresentationName>Diaformin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Diaformin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdiafo10922</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-06 15:27:04.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>MF 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73806-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>73808</Austr>
				<PresentationName>Diaformin</PresentationName>
    			<PresentionStrength>850mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Diaformin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdiafo10922</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-06 15:27:04.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>MF 2</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>73808-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>73808-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>82207</Austr>
				<PresentationName>Diaformin</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Diaformin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdiafo10922</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-06 15:27:04.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MF 3</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82207-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Diamicron</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>154042</Austr>
				<PresentationName>Diamicron MR</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gliclazide</TGAIngredient>
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			<brandname>Diane</brandname>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Lozenges</DoseForm>
							<Colour>brownish yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>233121-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>233121-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>233122</Austr>
				<PresentationName>Pharmacy Action Lozenges Orange</PresentationName>
    			<PresentionStrength>1.2mg/600mcg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/05/2017 17:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Lozenges</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>233122-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>233122-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Diclofenac Sodium (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>188546</Austr>
				<PresentationName>Diclofenac AN</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/11/2017 16:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown-yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>188546-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>188547</Austr>
				<PresentationName>Diclofenac AN</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/11/2017 16:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown-yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>188547-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Diclofenac Sodium (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>160729</Austr>
				<PresentationName>Apo-Diclofenac</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Diclofenac sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/05/2010 10:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown-yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>160729-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>160730</Austr>
				<PresentationName>Apo-Diclofenac</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Diclofenac sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/04/2010 15:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown-yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>160730-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Diclofenac Sodium (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>68940</Austr>
				<PresentationName>Diclofenac-GA</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 14:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown-yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>68940-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Diclofenac Sodium (GenRx)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>78432</Austr>
				<PresentationName>GenRx Diclofenac</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Diclofenac sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/08/2008 08:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown-yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>78432-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>78433</Austr>
				<PresentationName>GenRx Diclofenac</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Diclofenac sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/08/2008 08:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown-yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>78433-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Diclofenac Sodium (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>61297</Austr>
				<PresentationName>Diclofenac Sandoz</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Diclofenac sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 14:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown-yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>61297-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>61298</Austr>
				<PresentationName>Diclofenac Sandoz</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Diclofenac sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 14:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown-yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>61298-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>63661</Austr>
				<PresentationName>Diclofenac Sandoz</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Diclofenac sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 12:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown-yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>63661-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>63664</Austr>
				<PresentationName>Diclofenac Sandoz</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Diclofenac sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 12:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown-yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>63664-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dicloxacillin sodium (Viatris)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>289105</Austr>
				<PresentationName>Dicloxacillin Viatris</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Dicloxacillin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dicloxacillin Viatris</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdiclm11122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>dicloxacillin sodium</ActiveIngredient>
						<ReleaseDate>2022-11-28 10:33:22.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/12/2018 14:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>DX</Side1Marking>
							<Side2Marking>250</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>289105-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>289107</Austr>
				<PresentationName>Dicloxacillin Viatris</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Dicloxacillin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dicloxacillin Viatris</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdiclm11122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>dicloxacillin sodium</ActiveIngredient>
						<ReleaseDate>2022-11-28 10:33:22.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/12/2018 14:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>DX</Side1Marking>
							<Side2Marking>500</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>289107-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Difflam</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>132931</Austr>
				<PresentationName>Difflam Anaesthetic, Anti-Inflammatory, Anti-Bacterial Berry S/F</PresentationName>
    			<PresentionStrength>4mg/3mg/1.2mg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/03/2010 09:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Lozenges</DoseForm>
							<Colour>colourless</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>132931-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>132931-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>133507</Austr>
				<PresentationName>Difflam Anaesthetic, Anti-Inflammatory, Anti-Bacterial Menthol &amp; Eucalyptus S/F</PresentationName>
    			<PresentionStrength>4mg/3mg/1.2mg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/03/2010 09:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Lozenges</DoseForm>
							<Colour>pale blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>133507-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>133507-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>51468</Austr>
				<PresentationName>Difflam Sugar Free Raspberry</PresentationName>
    			<PresentionStrength>3mg/1.33mg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/03/2010 09:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Lozenges</DoseForm>
							<Colour>red-pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>51468-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>51468-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>53815</Austr>
				<PresentationName>Difflam Sugar Free Eucalyptus &amp; Menthol</PresentationName>
    			<PresentionStrength>3mg/1.33mg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/03/2010 09:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Lozenges</DoseForm>
							<Colour>pale blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>53815-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>53815-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>58319</Austr>
				<PresentationName>Difflam Sugar Free Doublemint</PresentationName>
    			<PresentionStrength>3mg/1.33mg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/03/2010 09:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Lozenges</DoseForm>
							<Colour>green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>58319-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>58319-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>58320</Austr>
				<PresentationName>Difflam Sugar Free Blackcurrant Cough</PresentationName>
    			<PresentionStrength>1.5mg/5.5mg/1.33mg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/03/2010 09:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Lozenges</DoseForm>
							<Colour>pink to lilac</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>58320-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>58320-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>72150</Austr>
				<PresentationName>Difflam Sugar Free Honey Lemon</PresentationName>
    			<PresentionStrength>3mg/1.33mg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/03/2010 09:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Lozenges</DoseForm>
							<Colour>lemon yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>72150-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>72150-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>72151</Austr>
				<PresentationName>Difflam Sugar Free Orange</PresentationName>
    			<PresentionStrength>3mg/1.33mg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/03/2010 09:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Lozenges</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>72151-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>72151-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dificid</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>195623</Austr>
				<PresentationName>Dificid</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Fidaxomicin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dificid</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>mkcdific10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fidaxomicin</ActiveIngredient>
						<ReleaseDate>2022-06-22 09:14:46.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/11/2016 09:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>FDX</Side1Marking>
							<Side2Marking>200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195623-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Diflucan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>48397</Austr>
				<PresentationName>Diflucan</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluconazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Diflucan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcdiflb10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fluconazole</ActiveIngredient>
						<ReleaseDate>2022-08-03 14:41:25.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/08/2008 13:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>purple/white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Pfizer</Side1Marking>
							<Side2Marking>FLU-200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>48397-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>48399</Austr>
				<PresentationName>Diflucan</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluconazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Diflucan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcdiflb10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fluconazole</ActiveIngredient>
						<ReleaseDate>2022-08-03 14:41:25.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/08/2008 13:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light turquoise blue/white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Pfizer</Side1Marking>
							<Side2Marking>FLU-50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>48399-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>48401</Austr>
				<PresentationName>Diflucan</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluconazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Diflucan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcdiflb10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fluconazole</ActiveIngredient>
						<ReleaseDate>2022-08-03 14:41:25.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/05/2021 10:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>standard blue/white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Pfizer</Side1Marking>
							<Side2Marking>FLU-100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>48401-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dilantin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>14305</Austr>
				<PresentationName>Dilantin</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Phenytoin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/09/2008 16:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>PARKE DAVIS</Side1Marking>
							<Side2Marking>P-D 100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>14305-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>14306</Austr>
				<PresentationName>Dilantin</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Phenytoin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/08/2008 13:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>PARKE DAVIS</Side1Marking>
							<Side2Marking>P-D 30</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>14306-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>14308</Austr>
				<PresentationName>Dilantin</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Phenytoin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/09/2011 10:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>triangular</Shape>
							<Side1Marking>P-D 007</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>14308-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>14308-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>295264</Austr>
				<PresentationName>Dilantin</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Phenytoin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dilantin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocdilaa11122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>phenytoin sodium</ActiveIngredient>
						<ReleaseDate>2022-11-30 15:43:40.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/05/2022 13:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>PARKE DAVIS</Side1Marking>
							<Side2Marking>P-D 30</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>295264-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>295265</Austr>
				<PresentationName>Dilantin</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Phenytoin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dilantin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocdilaa11122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>phenytoin sodium</ActiveIngredient>
						<ReleaseDate>2022-11-30 15:43:40.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/05/2022 13:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>PARKE DAVIS</Side1Marking>
							<Side2Marking>P-D 100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>295265-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>297268</Austr>
				<PresentationName>Dilantin</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Phenytoin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dilantin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocdilaa11122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>phenytoin sodium</ActiveIngredient>
						<ReleaseDate>2022-11-30 15:43:40.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/05/2022 13:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>triangular</Shape>
							<Side1Marking>P-D 007</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>297268-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>297268-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dilart</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167421</Austr>
				<PresentationName>Dilart</PresentationName>
    			<PresentionStrength>320mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dilart</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdilat10620</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>valsartan</ActiveIngredient>
						<ReleaseDate>2020-06-23 08:55:08.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/10/2016 14:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark grey</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>VN 4</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167421-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>167425</Austr>
				<PresentationName>Dilart</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dilart</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdilat10620</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>valsartan</ActiveIngredient>
						<ReleaseDate>2020-06-23 08:55:08.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/10/2016 14:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>VN 1</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167425-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>167426</Austr>
				<PresentationName>Dilart</PresentationName>
    			<PresentionStrength>160mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dilart</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdilat10620</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>valsartan</ActiveIngredient>
						<ReleaseDate>2020-06-23 08:55:08.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/10/2016 14:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>VN 3</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167426-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>167427</Austr>
				<PresentationName>Dilart</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dilart</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdilat10620</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>valsartan</ActiveIngredient>
						<ReleaseDate>2020-06-23 08:55:08.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/10/2016 14:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale red</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>M VN 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167427-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dilart HCT</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>187397</Austr>
				<PresentationName>Dilart HCT</PresentationName>
    			<PresentionStrength>80/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dilart HCT</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdilah10122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>valsartan with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2022-01-25 07:14:03.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/10/2016 14:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>VH 1</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>187397-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>187399</Austr>
				<PresentationName>Dilart HCT</PresentationName>
    			<PresentionStrength>320/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dilart HCT</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdilah10122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>valsartan with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2022-01-25 07:14:03.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/03/2018 12:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>VH 5</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>187399-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>187400</Austr>
				<PresentationName>Dilart HCT</PresentationName>
    			<PresentionStrength>160/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dilart HCT</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdilah10122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>valsartan with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2022-01-25 07:14:03.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/10/2016 14:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>VH 3</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>187400-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>187402</Austr>
				<PresentationName>Dilart HCT</PresentationName>
    			<PresentionStrength>320/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dilart HCT</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdilah10122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>valsartan with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2022-01-25 07:14:03.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/10/2016 14:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>VH 4</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>187402-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>187403</Austr>
				<PresentationName>Dilart HCT</PresentationName>
    			<PresentionStrength>160/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dilart HCT</DocumentName>
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   				<WithdrawalDate></WithdrawalDate>
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				<Austr>61106</Austr>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>131298-C01-02-BL600.jpg</ImageFileName>
							</View>
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			<Presentations>
				<Austr>131300</Austr>
				<PresentationName>Diltiazem Sandoz CD</PresentationName>
    			<PresentionStrength>240mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Diltiazem hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>diltiazem hydrochloride</ActiveIngredient>
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						<DateEffective>20/07/2012 11:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</View>
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			</Presentations>
			<Presentations>
				<Austr>131304</Austr>
				<PresentationName>Diltiazem Sandoz CD</PresentationName>
    			<PresentionStrength>360mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Diltiazem hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Diltiazem Sandoz CD</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>diltiazem hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-10-13 12:01:02.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 14:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and light blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>60838</Austr>
				<PresentationName>Diltiazem Sandoz</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Diltiazem hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 14:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>60838-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>62646</Austr>
				<PresentationName>Diltiazem Sandoz</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Diltiazem hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 14:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62646-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Diltiazem Hydrochloride (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>73851</Austr>
				<PresentationName>Terry White Chemists Diltiazem Tablets</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Diltiazem hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/08/2008 09:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>APO D60</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dilzem</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>50592</Austr>
				<PresentationName>Dilzem</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>23/02/2009 12:11</DateEffective>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>DL 60</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dimetapp</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>137255</Austr>
				<PresentationName>Dimetapp Daytime/Nightime Liquid Capsules</PresentationName>
    			<PresentionStrength></PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>Dimetapp</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>137255-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>Dimetapp</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>145584</Austr>
				<PresentationName>Dimetapp PE Nasal Decongestant Liquid Caps</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>12/02/2010 14:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>clear natural</Colour>
							<Scoring></Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>58352</Austr>
				<PresentationName>Dimetapp PSE Cough, Cold + Flu Day + Night</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
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							<Scoring></Scoring>
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							<View>
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							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>clear blue</Colour>
							<Scoring></Scoring>
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							<Side2Marking></Side2Marking>
							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>58353</Austr>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
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							<Scoring></Scoring>
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							<View>
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			<Presentations>
				<Austr>66743</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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							<View>
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		</Brand><Brand>
			<brandname>Dimetriose</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>50583</Austr>
				<PresentationName>Dimetriose</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient>Gestrinone</TGAIngredient>
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							<Side1Marking>Roussel logo</Side1Marking>
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							<View>
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			</Presentations>
		</Brand><Brand>
			<brandname>Dimirel</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>94474</Austr>
				<PresentationName>Dimirel</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Glimepiride</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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						<ActiveIngredient>glimepiride</ActiveIngredient>
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							<DoseForm>Tablets</DoseForm>
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			<Presentations>
				<Austr>94476</Austr>
				<PresentationName>Dimirel</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<ActiveIngredient>glimepiride</ActiveIngredient>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>94477</Austr>
				<PresentationName>Dimirel</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Glimepiride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dimirel</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcdimir10816</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>glimepiride</ActiveIngredient>
						<ReleaseDate>2016-08-29 17:25:34.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>NMN Hoechst logo</Side1Marking>
							<Side2Marking>NMN Hoechst logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>94477-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>94478</Austr>
				<PresentationName>Dimirel</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Glimepiride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dimirel</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcdimir10816</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>glimepiride</ActiveIngredient>
						<ReleaseDate>2016-08-29 17:25:34.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>NMO Hoechst logo</Side1Marking>
							<Side2Marking>NMO Hoechst logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>94478-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Diovan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>123357</Austr>
				<PresentationName>Diovan</PresentationName>
    			<PresentionStrength>320mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Diovan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcdvnor10220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>valsartan</ActiveIngredient>
						<ReleaseDate>2020-03-02 16:08:49.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/01/2011 13:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>grey-violet</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>DXL</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>123357-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>80868</Austr>
				<PresentationName>Diovan</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Diovan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcdvnor10220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>valsartan</ActiveIngredient>
						<ReleaseDate>2020-03-02 16:08:49.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/04/2009 10:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale red</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>D V</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>80868-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>80871</Austr>
				<PresentationName>Diovan</PresentationName>
    			<PresentionStrength>160mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Diovan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcdvnor10220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>valsartan</ActiveIngredient>
						<ReleaseDate>2020-03-02 16:08:49.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/04/2009 10:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>grey-orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>DX DX</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>80871-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>93165</Austr>
				<PresentationName>Diovan</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Diovan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcdvnor10220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>valsartan</ActiveIngredient>
						<ReleaseDate>2020-03-02 16:08:49.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/01/2011 13:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>D O</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>93165-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dipentum</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>14466</Austr>
				<PresentationName>Dipentum</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>olsalazine sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dipentum</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>iycdipen11116</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>olsalazine sodium</ActiveIngredient>
						<ReleaseDate>2016-11-16 14:15:03.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/10/2008 12:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>beige</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>DIPENTUM&#174; 250mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>14466-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>53582</Austr>
				<PresentationName>Dipentum</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>olsalazine sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dipentum</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>iycdipen11116</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>olsalazine sodium</ActiveIngredient>
						<ReleaseDate>2016-11-16 14:15:03.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/10/2008 12:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>D500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>53582-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Disprin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10021</Austr>
				<PresentationName>Disprin Forte</PresentationName>
    			<PresentionStrength>500mg/9.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/03/2011 12:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>D sword F</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>10021-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>10021-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>15356</Austr>
				<PresentationName>Disprin Chewable</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/03/2011 12:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>sword</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>15356-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>15356-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>53682</Austr>
				<PresentationName>Disprin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/03/2011 12:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>D sword X</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>53682-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>53682-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>59901</Austr>
				<PresentationName>Disprin</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/03/2011 12:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DISPRIN sword</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>59901-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>59901-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Distaph</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>59653</Austr>
				<PresentationName>Distaph</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Dicloxacillin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>DX</Side1Marking>
							<Side2Marking>500</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>59653-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>59655</Austr>
				<PresentationName>Distaph</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Dicloxacillin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>DX</Side1Marking>
							<Side2Marking>250</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>59655-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dithiazide</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>92060</Austr>
				<PresentationName>Dithiazide</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/01/2010 15:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Z 2083</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>92060-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ditropan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>48965</Austr>
				<PresentationName>Ditropan</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Oxybutynin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Ditropan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcditro10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>oxybutynin</ActiveIngredient>
						<ReleaseDate>2022-08-05 16:35:04.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/12/2010 11:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>48965-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dizole</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>132789</Austr>
				<PresentationName>Dizole</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluconazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dizole</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdizol11122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fluconazole</ActiveIngredient>
						<ReleaseDate>2022-11-11 16:10:36.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2010 14:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>G</Side1Marking>
							<Side2Marking>FC 200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>132789-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>159620</Austr>
				<PresentationName>Dizole</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluconazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dizole</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdizol11122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fluconazole</ActiveIngredient>
						<ReleaseDate>2022-11-11 16:10:36.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2010 14:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>G</Side1Marking>
							<Side2Marking>FC 100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159620-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>162640</Austr>
				<PresentationName>Dizole</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluconazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dizole</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdizol11122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fluconazole</ActiveIngredient>
						<ReleaseDate>2022-11-11 16:10:36.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/04/2011 14:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and dark blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>G</Side1Marking>
							<Side2Marking>FC 50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>162640-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>162766</Austr>
				<PresentationName>Dizole One</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>fluconazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dizole One</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdizon10322</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fluconazole</ActiveIngredient>
						<ReleaseDate>2022-03-14 07:51:11.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/07/2011 13:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsule</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>G</Side1Marking>
							<Side2Marking>FC 150</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>162766-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>96495</Austr>
				<PresentationName>Dizole</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluconazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2010 14:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>G</Side1Marking>
							<Side2Marking>FC 100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96495-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dolaforte</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>94737</Austr>
				<PresentationName>Dolaforte</PresentationName>
    			<PresentionStrength>30mg/500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-10 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>P500 C30</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>94737-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dolapril</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>125432</Austr>
				<PresentationName>Dolapril</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/03/2010 11:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TN 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>125432-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>125433</Austr>
				<PresentationName>Dolapril</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/03/2010 11:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>scarlet and peach opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TN 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>125433-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>125434</Austr>
				<PresentationName>Dolapril</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/03/2010 11:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>scarlet opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TN 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>125434-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>125435</Austr>
				<PresentationName>Dolapril</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/03/2010 11:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TN 4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>125435-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Doloxene</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>14630</Austr>
				<PresentationName>Doloxene</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/07/2009 08:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>pink</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>14630-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>161853</Austr>
				<PresentationName>Doloxene</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Dextropropoxyphene napsylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/08/2010 15:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>pink</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>161853-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Domperidone Maleate (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>242333</Austr>
				<PresentationName>APO-Domperidone</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>domperidone maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/12/2016 10:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Dm 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>242333-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Donepezil (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>193666</Austr>
				<PresentationName>Donepezil-GA</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 10:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C</Side1Marking>
							<Side2Marking>6</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>193666-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>193668</Austr>
				<PresentationName>Donepezil-GA</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 10:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C</Side1Marking>
							<Side2Marking>7</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>193668-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Donepezil hydrochloride (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167191</Austr>
				<PresentationName>Donepezil AN</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167191-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>167192</Austr>
				<PresentationName>Donepezil AN</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167192-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Donepezil hydrochloride (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>168327</Austr>
				<PresentationName>APO-Donepezil</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Donepezil hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DO 5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>168327-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>168328</Austr>
				<PresentationName>APO-Donepezil</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Donepezil hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow to yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DO 10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>168328-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>213495</Austr>
				<PresentationName>APO-Donepezil</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Donepezil hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/01/2015 09:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>C</Side1Marking>
							<Side2Marking>7</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>213495-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>213496</Austr>
				<PresentationName>APO-Donepezil</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Donepezil hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/01/2015 09:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow to yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>C</Side1Marking>
							<Side2Marking>6</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>213496-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Donepezil hydrochloride (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>168330</Austr>
				<PresentationName>Chemmart Donepezil</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Donepezil hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DO 5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>168330-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>168337</Austr>
				<PresentationName>Chemmart Donepezil</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Donepezil hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow to yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DO 10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>168337-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>213497</Austr>
				<PresentationName>Chemmart Donepezil</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Donepezil hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 10:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>C</Side1Marking>
							<Side2Marking>7</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>213497-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>213498</Austr>
				<PresentationName>Chemmart Donepezil</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Donepezil hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 10:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow to yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>C</Side1Marking>
							<Side2Marking>6</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>213498-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Donepezil hydrochloride (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>172750</Austr>
				<PresentationName>Donepezil generichealth</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 11:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>RC 25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>172750-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>172753</Austr>
				<PresentationName>Donepezil generichealth</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 11:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>RC 26</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>172753-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Donepezil hydrochloride (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167194</Austr>
				<PresentationName>Pharmacor Donepezil </PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/10/2013 11:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167194-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>167195</Austr>
				<PresentationName>Pharmacor Donepezil</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/10/2013 11:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167195-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Donepezil hydrochloride (Ranbaxy)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>172754</Austr>
				<PresentationName>Donepezil RBX</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/09/2013 16:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>RC 26</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>172754-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Donepezil hydrochloride (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>157837</Austr>
				<PresentationName>Donepezil Sandoz</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Donepezil hydrochloride monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/08/2013 14:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157837-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>157842</Austr>
				<PresentationName>Donepezil Sandoz</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Donepezil hydrochloride monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/08/2013 14:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157842-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Donepezil hydrochloride (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>168329</Austr>
				<PresentationName>Terry White Chemists Donepezil</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Donepezil hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DO 5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>168329-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>168336</Austr>
				<PresentationName>Terry White Chemists Donepezil</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Donepezil hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow to yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DO 10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>168336-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>213499</Austr>
				<PresentationName>Terry White Chemists Donepezil</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Donepezil hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>C</Side1Marking>
							<Side2Marking>7</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>213499-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>213500</Austr>
				<PresentationName>Terry White Chemists Donepezil</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Donepezil hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow to yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>C</Side1Marking>
							<Side2Marking>6</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>213500-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Donnatab</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>60604</Austr>
				<PresentationName>Donnatab</PresentationName>
    			<PresentionStrength>103.7/19.4/6.5mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/02/2010 14:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>R</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>60604-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dormizol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>117953</Austr>
				<PresentationName>Dormizol</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Zolpidem tartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dormizol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcdormi10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>zolpidem tartrate</ActiveIngredient>
						<ReleaseDate>2022-06-02 11:06:02.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/07/2008 10:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>SN 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>117953-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Doryx</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>29728</Austr>
				<PresentationName>Doryx</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Doryx</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>yncdoryx40519</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>doxycycline hyclate (hydrochloride)</ActiveIngredient>
						<ReleaseDate>2019-07-05 09:45:09.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/03/2011 18:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>clear</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Doryx</Side1Marking>
							<Side2Marking>50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>29728-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>30100</Austr>
				<PresentationName>Doryx</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Doryx</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>yncdoryx40519</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>doxycycline hyclate (hydrochloride)</ActiveIngredient>
						<ReleaseDate>2019-07-05 09:45:09.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/03/2011 18:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>clear</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Doryx</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>30100-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dostan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>170398</Austr>
				<PresentationName>Dostan</PresentationName>
    			<PresentionStrength>500mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Cabergoline</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/02/2011 14:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>700</Side1Marking>
							<Side2Marking>P U</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>170398-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dostinex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>52158</Austr>
				<PresentationName>Dostinex</PresentationName>
    			<PresentionStrength>500mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Cabergoline</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dostinex</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcdostt10720</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>cabergoline</ActiveIngredient>
						<ReleaseDate>2020-07-02 15:20:17.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/09/2011 10:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>700</Side1Marking>
							<Side2Marking>P U</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>52158-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>289783</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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						<DateEffective>20/12/2018 16:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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			<Presentations>
				<Austr>289784</Austr>
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    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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				<Documents>
					<DocumentQualifiers>
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							<AvailableFormats>
								<Format>PDF</Format>
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							<Side1Marking>DT 75</Side1Marking>
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			</Presentations>
		</Brand><Brand>
			<brandname>Dothep</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>34419</Austr>
				<PresentationName>Dothep</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Dothiepin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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				</Images>
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			<Presentations>
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				<PresentationName>Dothep</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<AvailableFormats>
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							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
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								<ImageFileName>62910-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
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			<brandname>Dovato</brandname>
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			<Presentations>
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    			<PresentionStrength>50mg/300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
				<Austr>148807</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<Views>
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			</Presentations>
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			<brandname>Doxy</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
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    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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			</Presentations>
			<Presentations>
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    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateEffective>23/02/2009 12:14</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
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							<Side2Marking></Side2Marking>
							<Views>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Doxycycline (Mayne Pharma)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>107247</Austr>
				<PresentationName>Mayne Doxycycline</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
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				<Documents>
					<DocumentQualifiers>
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						<QualiferData></QualiferData>
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						<DocumentTypes>
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							<AvailableFormats>
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						</DocumentTypes>
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				<Images>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Capsules</DoseForm>
							<Colour>clear</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>doxy</Side1Marking>
							<Side2Marking>50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>107247-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
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			</Presentations>
			<Presentations>
				<Austr>107248</Austr>
				<PresentationName>Mayne Doxycycline</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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							<AvailableFormats>
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						</DocumentTypes>
						<ActiveIngredient>doxycycline hyclate (hydrochloride)</ActiveIngredient>
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				<Images>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<Scoring></Scoring>
							<Shape></Shape>
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							<Views>
							<View>
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			<Presentations>
				<Austr>78597</Austr>
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    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Colour>dull yellow</Colour>
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							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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			<Presentations>
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    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
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    			<TGAIngredient>Doxycycline monohydrate</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<Colour>dull yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
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							<Views>
							<View>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient>Doxycycline monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 15:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dull yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>66302-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>69049</Austr>
				<PresentationName>Doxycycline Sandoz</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Doxycycline monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 15:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dull yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>69049-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Doxylamine Succinate (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>204244</Austr>
				<PresentationName>Pharmacy Action Sleep Aid</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 10:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204244-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Doxylin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>63509</Austr>
				<PresentationName>Doxylin</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Doxycycline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Doxylin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdoxyl10520</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>doxycycline</ActiveIngredient>
						<ReleaseDate>2020-05-13 15:06:59.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DE 100</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>63509-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>63512</Austr>
				<PresentationName>Doxylin</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Doxycycline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Doxylin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcdoxyl10520</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>doxycycline</ActiveIngredient>
						<ReleaseDate>2020-05-13 15:06:59.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DE 50</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>63512-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Duavive</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>262525</Austr>
				<PresentationName>Duavive</PresentationName>
    			<PresentionStrength>0.45mg/20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bazedoxifene acetate,conjugated estrogens</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Duavive</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcduavt10619</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>conjugated estrogens with bazedoxifene</ActiveIngredient>
						<ReleaseDate>2019-06-19 11:07:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/10/2017 11:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>0.45 / 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>262525-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Dulcolax (Sanofi)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>155405</Austr>
				<PresentationName>Dulcolax</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dulcolax Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcdultb10418</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>bisacodyl</ActiveIngredient>
						<ReleaseDate>2018-12-20 12:38:33.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>02/07/2014 10:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige-yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>155405-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>17926</Austr>
				<PresentationName>Dulcolax</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Suppositories</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Dulcolax Suppositories</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcdulsp10418</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>bisacodyl</ActiveIngredient>
						<ReleaseDate>2018-12-20 12:38:25.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/07/2010 10:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Suppositories</DoseForm>
							<Colour>white or slightly yellowish</Colour>
							<Scoring></Scoring>
							<Shape>torpedo</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>17926-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Duloxetine hydrochloride (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>199003</Austr>
				<PresentationName>Duloxetine AN</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue opaque and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>X</Side1Marking>
							<Side2Marking>02</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199003-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199011</Austr>
				<PresentationName>Duloxetine AN</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue opaque and green opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>X</Side1Marking>
							<Side2Marking>03</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199011-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Duloxetine hydrochloride (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>217985</Austr>
				<PresentationName>APO-Duloxetine</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Duloxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/01/2015 09:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue opaque and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>157</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>217985-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>217986</Austr>
				<PresentationName>APO-Duloxetine</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Duloxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/01/2015 09:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue opaque and green opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>158</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>217986-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Duloxetine hydrochloride (Chemmart)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>217987</Austr>
				<PresentationName>Chemmart Duloxetine</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Duloxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue opaque and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>157</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>217987-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>217988</Austr>
				<PresentationName>Chemmart Duloxetine</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Duloxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue opaque and green opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>158</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>217988-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Duloxetine hydrochloride (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>197150</Austr>
				<PresentationName>Duloxetine GH</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>dark blue and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>DU</Side1Marking>
							<Side2Marking>30</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
					</Versions>
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			</Presentations>
			<Presentations>
				<Austr>197151</Austr>
				<PresentationName>Duloxetine GH</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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						<DateEffective>01/10/2013 11:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>dark blue and green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>DU</Side1Marking>
							<Side2Marking>60</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>197151-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Duloxetine hydrochloride (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>209157</Austr>
				<PresentationName>Pharmacor Duloxetine</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque blue and opaque green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Dulox</Side1Marking>
							<Side2Marking>60 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>209157-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>209159</Austr>
				<PresentationName>Pharmacor Duloxetine</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>10/10/2016 09:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque blue and opaque white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Dulox</Side1Marking>
							<Side2Marking>30 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>209159-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Duloxetine hydrochloride (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>199254</Austr>
				<PresentationName>Duloxetine Sandoz</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>12/04/2018 09:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue and green opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>158</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199254-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199266</Austr>
				<PresentationName>Duloxetine Sandoz</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/04/2018 09:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>157</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199266-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Duloxetine hydrochloride (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>217989</Austr>
				<PresentationName>Terry White Chemists Duloxetine</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Duloxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue opaque and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>157</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>217989-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>217990</Austr>
				<PresentationName>Terry White Chemists Duloxetine</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Duloxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue opaque and green opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>158</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>217990-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Duocover</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>151075</Austr>
				<PresentationName>Duocover</PresentationName>
    			<PresentionStrength>75mg/100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clopidogrel hydrogen sulfate,Aspirin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>DuoCover</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clopidogrel with aspirin</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C75</Side1Marking>
							<Side2Marking>A100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151075-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Duodart</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>162530</Austr>
				<PresentationName>Duodart</PresentationName>
    			<PresentionStrength>500mcg/400mcg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Dutasteride,Tamsulosin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Duodart</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>dutasteride with tamsulosin hydrochloride</ActiveIngredient>
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				<Images>
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						<DateEffective>24/06/2011 15:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange and brown</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>GS 7CZ</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
		</Brand><Brand>
			<brandname>DuoPlidogrel</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>150480</Austr>
				<PresentationName>DuoPlidogrel</PresentationName>
    			<PresentionStrength>75mg/100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>aspirin,clopidogrel hydrogen sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Duoplidogrel</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>clopidogrel with aspirin</ActiveIngredient>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C75</Side1Marking>
							<Side2Marking>A100</Side2Marking>
							<Views>
							<View>
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		</Brand><Brand>
			<brandname>Duride</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>60907</Austr>
				<PresentationName>Duride</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Isosorbide mononitrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Duride</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>isosorbide mononitrate</ActiveIngredient>
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						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>IM 60</Side1Marking>
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							<Views>
							<View>
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		</Brand><Brand>
			<brandname>Duro-Tuss</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>159201</Austr>
				<PresentationName>Duro-Tuss Chesty Cough Sugar Free Lemon</PresentationName>
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    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Shape>round</Shape>
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							<View>
								<ViewLabel>B</ViewLabel>
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			<Presentations>
				<Austr>210274</Austr>
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    			<PresentionStrength>8mg/200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>B</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
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			<Presentations>
				<Austr>51466</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Lozenges</DoseForm>
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						<DateEffective>26/10/2022 13:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
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							<Side1Marking>DF1</Side1Marking>
							<Side2Marking>M</Side2Marking>
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								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>331686</Austr>
				<PresentationName>Eferas</PresentationName>
    			<PresentionStrength>90mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>deferasirox</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<ActiveIngredient>deferasirox</ActiveIngredient>
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						<DateEffective>26/10/2022 13:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>DF</Side1Marking>
							<Side2Marking>M</Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>331686-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>331687</Austr>
				<PresentationName>Eferas</PresentationName>
    			<PresentionStrength>360mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>deferasirox</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DateEffective>26/10/2022 13:42</DateEffective>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>DF2</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>331687-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Efexor</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>60858</Austr>
				<PresentationName>Efexor-XR</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Venlafaxine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Efexor XR</DocumentName>
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								<Format>PDF</Format>
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						<ActiveIngredient>venlafaxine hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-10-22 11:55:44.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/09/2011 10:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque peach</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>W</Side1Marking>
							<Side2Marking>75</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>60858-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>60859</Austr>
				<PresentationName>Efexor-XR</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Venlafaxine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Efexor XR</DocumentName>
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								<Format>PDF</Format>
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						<ActiveIngredient>venlafaxine hydrochloride</ActiveIngredient>
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					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque dark orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>W</Side1Marking>
							<Side2Marking>150</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>60859-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>99802</Austr>
				<PresentationName>Efexor-XR</PresentationName>
    			<PresentionStrength>37.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Venlafaxine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>venlafaxine hydrochloride</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/08/2008 12:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>grey and peach</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>W</Side1Marking>
							<Side2Marking>37.5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Elaxine SR</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>160299</Austr>
				<PresentationName>Elaxine SR</PresentationName>
    			<PresentionStrength>37.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>11/04/2018 15:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>grey/peach with red thick and thin circular bands</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
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			</Presentations>
			<Presentations>
				<Austr>160300</Austr>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/04/2018 15:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>peach with red thick and thin circular bands</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>160300-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>160301</Austr>
				<PresentationName>Elaxine SR</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>dark orange - white thick and thin circular bands</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>160301-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Eldepryl</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>47465</Austr>
				<PresentationName>Eldepryl</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Selegiline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>23/02/2009 12:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>47465-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Eleanor</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>205579</Austr>
				<PresentationName>Eleanor 150/30 ED</PresentationName>
    			<PresentionStrength>150mcg/30mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>07/12/2017 13:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>LE4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>205579-C01-01-BL600.jpg</ImageFileName>
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							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
		</Brand><Brand>
			<brandname>Eleva</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>95581</Austr>
				<PresentationName>Eleva</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sertraline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Eleva</DocumentName>
						<DocumentTypes>
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						<ActiveIngredient>sertraline hydrochloride</ActiveIngredient>
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				<Images>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>ST 50</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>95582</Austr>
				<PresentationName>Eleva</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Sertraline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Eleva</DocumentName>
						<DocumentTypes>
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						<ActiveIngredient>sertraline hydrochloride</ActiveIngredient>
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						<VersionSequence>1</VersionSequence>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
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							<View>
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			</Presentations>
			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sertraline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<ReleaseDate>2022-08-08 15:51:44.0</ReleaseDate>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>ST 100</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>95583-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>95584</Austr>
				<PresentationName>Eleva</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Sertraline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Eleva</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afceleva10822</Filename>
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						</DocumentTypes>
						<ActiveIngredient>sertraline hydrochloride</ActiveIngredient>
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						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/11/2022 12:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>ST 100</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>95584-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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			</Presentations>
		</Brand><Brand>
			<brandname>Elevit</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>79412</Austr>
				<PresentationName>Elevit</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2009 14:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>79412-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Elovax</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>204623</Austr>
				<PresentationName>Elovax</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>famciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/08/2013 14:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>FV 500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204623-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Emexlon</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>229659</Austr>
				<PresentationName>Emexlon</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/04/2018 15:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>229659-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>268301</Austr>
				<PresentationName>Emexlon</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/04/2018 15:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>268301-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Enablex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>99418</Austr>
				<PresentationName>Enablex</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Darifenacin hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/11/2008 12:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DF</Side1Marking>
							<Side2Marking>7.5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>99418-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>99439</Austr>
				<PresentationName>Enablex</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Darifenacin hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/11/2008 12:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light-peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DF</Side1Marking>
							<Side2Marking>15</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>99439-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Enalapril (GA)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>121953</Austr>
				<PresentationName>Enalapril-GA</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/07/2009 14:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121953-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121954</Austr>
				<PresentationName>Enalapril-GA</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/07/2009 14:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red-brown</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121954-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121955</Austr>
				<PresentationName>Enalapril-GA</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/07/2009 14:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>EN 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121955-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Enalapril Maleate (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>188553</Austr>
				<PresentationName>Enalapril AN</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red-brown</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>EN 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>188553-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Enalapril Maleate (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>196466</Austr>
				<PresentationName>APO-Enalapril</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Enalapril maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/01/2015 09:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>196472</Austr>
				<PresentationName>APO-Enalapril</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Enalapril maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 10:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>196472-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>196504</Austr>
				<PresentationName>APO-Enalapril</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Enalapril maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 10:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>196504-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Enalapril Maleate (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>142949</Austr>
				<PresentationName>Enalapril generichealth</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>barrel-shaped</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>142950</Austr>
				<PresentationName>Enalapril generichealth</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/04/2015 16:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>barrel-shaped</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>142950-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>142951</Austr>
				<PresentationName>Enalapril generichealth</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/04/2015 16:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>barrel-shaped</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>142951-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Enalapril Maleate (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>121813</Austr>
				<PresentationName>Enalapril Sandoz</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Enalapril maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/06/2010 13:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>EN 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121813-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121814</Austr>
				<PresentationName>Enalapril Sandoz</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Enalapril maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/06/2010 13:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red-brown</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>EN 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121814-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121816</Austr>
				<PresentationName>Enalapril Sandoz</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Enalapril maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/06/2010 13:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>EN 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121816-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Enalapril/HCT (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>126490</Austr>
				<PresentationName>Enalapril/HCT Sandoz</PresentationName>
    			<PresentionStrength>20mg/6mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Enalapril maleate,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>EN 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>126490-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Endep</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>59788</Austr>
				<PresentationName>Endep</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amitriptyline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Endep</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcendep10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amitriptyline hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-09-07 15:36:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AP 25</Side1Marking>
							<Side2Marking>&#945;</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>59788-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>64425</Austr>
				<PresentationName>Endep</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amitriptyline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Endep</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcendep10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amitriptyline hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-09-07 15:36:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>tan</Colour>
							<Scoring>unscored</Scoring>
							<Shape>six-sided</Shape>
							<Side1Marking>AP 50</Side1Marking>
							<Side2Marking>&#945;</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>64425-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>71044</Austr>
				<PresentationName>Endep</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amitriptyline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Endep</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcendep10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amitriptyline hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-09-07 15:36:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AP 10</Side1Marking>
							<Side2Marking>&#945;</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>71044-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Endometrin</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>189948</Austr>
				<PresentationName>Endometrin</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Pessaries</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Progesterone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Endometrin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fpcendov10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>progesterone</ActiveIngredient>
						<ReleaseDate>2022-09-28 12:50:08.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/07/2013 12:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Pessaries</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>FPI</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>189948-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>189948-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Endone</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>14945</Austr>
				<PresentationName>Endone</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>oxycodone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Endone</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocendon10422</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>oxycodone hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-04-06 10:37:18.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2022 15:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>O 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>14945-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Enlafax XR</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>143533</Austr>
				<PresentationName>Enlafax XR</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Venlafaxine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Enlafax XR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>venlafaxine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-01-28 10:48:35.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/03/2018 12:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque flesh-coloured</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>VEN</Side1Marking>
							<Side2Marking>75</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>143533-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>143552</Austr>
				<PresentationName>Enlafax XR</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Venlafaxine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Enlafax XR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcenlax10122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>venlafaxine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-01-28 10:48:35.0</ReleaseDate>
					</DocumentQualifiers>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/03/2018 12:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque scarlet-coloured</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>VEN</Side1Marking>
							<Side2Marking>150</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>143552-C01-02-BL600.jpg</ImageFileName>
							</View>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Entecavir monohydrate (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>217581</Austr>
				<PresentationName>Entecavir Apotex</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Entecavir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/07/2017 15:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>triangular</Shape>
							<Side1Marking>0.5 ENT</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>217581-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>217583</Austr>
				<PresentationName>Entecavir Apotex</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Entecavir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/07/2017 15:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>triangular</Shape>
							<Side1Marking>1 ENT</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>217583-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>256432</Austr>
				<PresentationName>Entecavir APO</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>entecavir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/10/2019 08:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>triangular</Shape>
							<Side1Marking>RL1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>256432-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>256492</Austr>
				<PresentationName>Entecavir APO</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>entecavir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/10/2019 08:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink to pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>triangular</Shape>
							<Side1Marking>RL2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>256492-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Entecavir monohydrate (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>227418</Austr>
				<PresentationName>Entecavir Sandoz</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Entecavir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/10/2017 14:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>109</Side1Marking>
							<Side2Marking>SZ</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>227418-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>227420</Austr>
				<PresentationName>Entecavir Sandoz</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Entecavir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/10/2017 14:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>108</Side1Marking>
							<Side2Marking>SZ</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>227420-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Entecavir monohydrate (Viatris)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>220090</Austr>
				<PresentationName>Entecavir Viatris</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>entecavir monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Entecavir Viatris</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcentem11122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>entecavir monohydrate</ActiveIngredient>
						<ReleaseDate>2022-11-07 13:54:50.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/12/2018 10:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>EV1</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>220090-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>220091</Austr>
				<PresentationName>Entecavir Viatris</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>entecavir monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Entecavir Viatris</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcentem11122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>entecavir monohydrate</ActiveIngredient>
						<ReleaseDate>2022-11-07 13:54:50.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/06/2019 06:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>EV2</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>220091-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Enteclude</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>259912</Austr>
				<PresentationName>Enteclude</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/11/2017 16:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>triangular</Shape>
							<Side1Marking>ENT</Side1Marking>
							<Side2Marking>0.5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>259912-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>259921</Austr>
				<PresentationName>Enteclude</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/11/2017 16:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>triangular</Shape>
							<Side1Marking>ENT</Side1Marking>
							<Side2Marking>1</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>259921-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Entocort</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>62812</Austr>
				<PresentationName>Entocort</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Budesonide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/08/2008 11:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light grey and pink</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>CIR 3 mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62812-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Entresto</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>234218</Austr>
				<PresentationName>Entresto</PresentationName>
    			<PresentionStrength>97mg/103mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>sacubitril,Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Entresto</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcentor31120</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>sacubitril with valsartan</ActiveIngredient>
						<ReleaseDate>2022-03-02 14:10:16.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/09/2016 10:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>ovaloid</Shape>
							<Side1Marking>L11</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234218-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>234219</Austr>
				<PresentationName>Entresto</PresentationName>
    			<PresentionStrength>24mg/26mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>sacubitril,Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Entresto</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcentor31120</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>sacubitril with valsartan</ActiveIngredient>
						<ReleaseDate>2022-03-02 14:10:16.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/09/2016 10:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>violet-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>ovaloid</Shape>
							<Side1Marking>LZ</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234219-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>234222</Austr>
				<PresentationName>Entresto</PresentationName>
    			<PresentionStrength>49mg/51mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>sacubitril,Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Entresto</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcentor31120</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>sacubitril with valsartan</ActiveIngredient>
						<ReleaseDate>2022-03-02 14:10:16.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/09/2016 10:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>ovaloid</Shape>
							<Side1Marking>L1</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234222-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Entrip</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>232152</Austr>
				<PresentationName>Entrip</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
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			<brandname>Epilim</brandname>
			<isamtbrand>true</isamtbrand>
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				<Austr>15369</Austr>
				<PresentationName>Epilim</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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			<Presentations>
				<Austr>15370</Austr>
				<PresentationName>Epilim</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sodium valproate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
				<Austr>15373</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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			<brandname>Epiramax</brandname>
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			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Eryc</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>yncerycc40920</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>erythromycin</ActiveIngredient>
						<ReleaseDate>2020-10-12 15:42:14.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>31/01/2013 13:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>transparent red/yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Eryc</Side1Marking>
							<Side2Marking>Eryc</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>63154-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>63156</Austr>
				<PresentationName>Eryc</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 16:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>transparent red/yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Eryc</Side1Marking>
							<Side2Marking>Eryc</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>63156-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Erythromycin (Mayne Pharma)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>195842</Austr>
				<PresentationName>Mayne Pharma Erythromycin</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Mayne Pharma Erythromycin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ynceryth40920</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>erythromycin</ActiveIngredient>
						<ReleaseDate>2020-10-12 15:42:22.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/02/2013 09:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>transparent red/yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Eryc</Side1Marking>
							<Side2Marking>Eryc</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195842-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>79999</Austr>
				<PresentationName>Mayne Pharma Erythromycin</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 16:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>transparent red/yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Eryc</Side1Marking>
							<Side2Marking>Eryc</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>79999-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Escicor</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>166139</Austr>
				<PresentationName>Escicor 10</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/09/2013 16:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166139-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166140</Austr>
				<PresentationName>Escicor 20</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/09/2013 16:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166140-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Escitalopram (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>190287</Austr>
				<PresentationName>Escitalopram AN</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>190287-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>190288</Austr>
				<PresentationName>Escitalopram AN</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>190288-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Escitalopram (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>146007</Austr>
				<PresentationName>Apo-Escitalopram</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Escitalopram oxalate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/02/2010 10:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ESC 10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>146007-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>146015</Austr>
				<PresentationName>Apo-Escitalopram</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Escitalopram oxalate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/02/2010 09:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ESC 20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>146015-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>213721</Austr>
				<PresentationName>APO-Escitalopram </PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Escitalopram oxalate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 10:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>213721-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>213722</Austr>
				<PresentationName>APO-Escitalopram </PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Escitalopram oxalate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 10:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>213722-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Escitalopram (Blooms the Chemist)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>272630</Austr>
				<PresentationName>Blooms the Chemist Escitalopram</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>escitalopram oxalate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/05/2017 11:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>272630-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>272631</Austr>
				<PresentationName>Blooms the Chemist Escitalopram</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>escitalopram oxalate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/05/2017 11:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>272631-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Escitalopram (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>146023</Austr>
				<PresentationName>Chemmart Escitalopram</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Escitalopram oxalate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2010 14:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ESC 10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>146023-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>146027</Austr>
				<PresentationName>Chemmart Escitalopram</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Escitalopram oxalate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
				<Austr>165431</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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			<brandname>Escitalopram (Generic Health)</brandname>
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			<Presentations>
				<Austr>165848</Austr>
				<PresentationName>Escitalopram generichealth</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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			<Presentations>
				<Austr>165880</Austr>
				<PresentationName>Escitalopram generichealth</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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			<brandname>Escitalopram (Pharmacor)</brandname>
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			<Presentations>
				<Austr>166137</Austr>
				<PresentationName>Pharmacor Escitalopram</PresentationName>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<brandname>Escitalopram (Terry White Chemists)</brandname>
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		</Brand><Brand>
			<brandname>Esitalo</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>146907</Austr>
				<PresentationName>Esitalo</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pneumococcal purified capsular polysaccharides</TGAIngredient>
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								<ViewLabel>C</ViewLabel>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
		</Brand><Brand>
			<brandname>Eskazole</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>97505</Austr>
				<PresentationName>Eskazole</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient>Albendazole</TGAIngredient>
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							<Side1Marking>ALB 400</Side1Marking>
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								<ViewLabel>C</ViewLabel>
								<ImageFileName>97505-C01-01-BL600.jpg</ImageFileName>
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		</Brand><Brand>
			<brandname>Esomeprazole (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>206009</Austr>
				<PresentationName>Esomeprazole Actavis</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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							<PhaseItem>1</PhaseItem>
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							<Colour>opaque yellow and opaque white</Colour>
							<Scoring></Scoring>
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							<Side2Marking>20 mg</Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>206009-C01-01-BL600.jpg</ImageFileName>
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   				<WithdrawalDate></WithdrawalDate>
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							<Shape></Shape>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>206014-C01-01-BL600.jpg</ImageFileName>
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			<brandname>Esomeprazole (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>210843</Austr>
				<PresentationName>Esomeprazole APOTEX</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Side2Marking></Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
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			<Presentations>
				<Austr>210849</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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							<Scoring>unscored</Scoring>
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							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>210849-C01-01-BL600.jpg</ImageFileName>
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		</Brand><Brand>
			<brandname>Esomeprazole (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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							<Side1Marking>CE</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>207588-C01-01-BL600.jpg</ImageFileName>
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			<brandname>Esomeprazole (GxP)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>205831</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
				<Austr>297505</Austr>
				<PresentationName>Everolimus Sandoz</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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							<Side1Marking>UHE</Side1Marking>
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			<brandname>Evifyne</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>172550</Austr>
				<PresentationName>Evifyne</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-02-02 00:00:00'}</WithdrawalDate>
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							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>4165</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>172550-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
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			</Presentations>
		</Brand><Brand>
			<brandname>Evista</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>64709</Austr>
				<PresentationName>Evista</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<DocumentQualifiers>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<DateEffective>13/10/2008 11:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>4165</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>64709-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Exaccord</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167856</Austr>
				<PresentationName>Exaccord</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateEffective>12/09/2011 09:23</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>E25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167856-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Exelon</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>71445</Austr>
				<PresentationName>Exelon</PresentationName>
    			<PresentionStrength>1.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rivastigmine hydrogen tartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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								<Format>PDF</Format>
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						<ActiveIngredient>rivastigmine hydrogen tartrate</ActiveIngredient>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
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							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>EXELON 1,5 mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>71445-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>71446</Austr>
				<PresentationName>Exelon</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rivastigmine hydrogen tartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Exelon</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>rivastigmine hydrogen tartrate</ActiveIngredient>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/11/2008 13:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>EXELON 3 mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>71446-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>71447</Austr>
				<PresentationName>Exelon</PresentationName>
    			<PresentionStrength>4.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rivastigmine hydrogen tartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>rivastigmine hydrogen tartrate</ActiveIngredient>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
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							<Colour>red</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>EXELON 4,5 mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>71448</Austr>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rivastigmine hydrogen tartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<DocumentQualifiers>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>EXELON 6 mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			<brandname>Exemestane (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>177311</Austr>
				<PresentationName>Exemestane AN</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
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							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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			<brandname>Exemestane (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>177312</Austr>
				<PresentationName>APO-Exemestane</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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							<DoseForm>Tablets</DoseForm>
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							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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				</Images>
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		</Brand><Brand>
			<brandname>Exemestane (GA)</brandname>
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			<Presentations>
				<Austr>167857</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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			<brandname>Exemestane (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167858</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient></TGAIngredient>
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			<brandname>Exemestane (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>174337</Austr>
				<PresentationName>Exemestane Sandoz</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan,Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
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							<Side2Marking>NVR</Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>130834</Austr>
				<PresentationName>Exforge</PresentationName>
    			<PresentionStrength>5mg/160mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan,Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Exforge</DocumentName>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>ECE</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>130834-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>130841</Austr>
				<PresentationName>Exforge</PresentationName>
    			<PresentionStrength>10mg/160mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan,Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Exforge</DocumentName>
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						<ActiveIngredient>amlodipine besilate with valsartan</ActiveIngredient>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/05/2009 13:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>UIC</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>130841-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>157954</Austr>
				<PresentationName>Exforge HCT</PresentationName>
    			<PresentionStrength>5mg/160mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Valsartan,Hydrochlorothiazide,Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Exforge HCT</DocumentName>
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							<DocumentType>eCMI</DocumentType>
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								<Format>PDF</Format>
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						<ActiveIngredient>amlodipine besilate with valsartan and hydrochlorothiazide</ActiveIngredient>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/01/2011 09:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>ovaloid</Shape>
							<Side1Marking>VCL</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157954-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158162</Austr>
				<PresentationName>Exforge HCT</PresentationName>
    			<PresentionStrength>5mg/160mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Hydrochlorothiazide,Amlodipine besylate,Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Exforge HCT</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
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								<Format>PDF</Format>
								<Filename>nvcexfhc11022</Filename>
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						<ActiveIngredient>amlodipine besilate with valsartan and hydrochlorothiazide</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/01/2011 09:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>ovaloid</Shape>
							<Side1Marking>VEL</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158162-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158164</Austr>
				<PresentationName>Exforge HCT</PresentationName>
    			<PresentionStrength>10mg/160mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Valsartan,Hydrochlorothiazide,Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Exforge HCT</DocumentName>
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							<DocumentType>eCMI</DocumentType>
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								<Format>PDF</Format>
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						<ActiveIngredient>amlodipine besilate with valsartan and hydrochlorothiazide</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>20/01/2011 09:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>ovaloid</Shape>
							<Side1Marking>VDL</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>158166</Austr>
				<PresentationName>Exforge HCT</PresentationName>
    			<PresentionStrength>10mg/160mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Amlodipine besylate,Hydrochlorothiazide,Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Exforge HCT</DocumentName>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown yellow</Colour>
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							<Shape>ovaloid</Shape>
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							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>158168</Austr>
				<PresentationName>Exforge HCT</PresentationName>
    			<PresentionStrength>10mg/320mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Amlodipine besylate,Hydrochlorothiazide,Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Exforge HCT</DocumentName>
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							<DocumentType>eCMI</DocumentType>
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						<ActiveIngredient>amlodipine besilate with valsartan and hydrochlorothiazide</ActiveIngredient>
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						<VersionSequence>1</VersionSequence>
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						<DateEffective>20/01/2011 09:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>ovaloid</Shape>
							<Side1Marking>VFL</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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			<Presentations>
				<Austr>161820</Austr>
				<PresentationName>Exforge</PresentationName>
    			<PresentionStrength>5mg/320mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Amlodipine besylate,Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Exforge</DocumentName>
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							<DocumentType>eCMI</DocumentType>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<View>
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			<Presentations>
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    			<PresentionStrength>10mg/320mg</PresentionStrength>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Valsartan,Amlodipine besylate</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<QualifierType></QualifierType>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
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							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
		</Brand><Brand>
			<brandname>Extine</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>120729</Austr>
				<PresentationName>Extine</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
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						<DateEffective>11/04/2018 16:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>X T</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>120729-C01-02-BL600.jpg</ImageFileName>
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						</Phase>
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			</Presentations>
		</Brand><Brand>
			<brandname>Ezalo</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>203688</Austr>
				<PresentationName>Ezalo</PresentationName>
    			<PresentionStrength>10mg/40mg</PresentionStrength>
    			<PresentationForm>Pack</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>composite pack</Container>
    			<TGAIngredient>Rosuvastatin calcium,Ezetimibe</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Ezalo Composite Pack</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>ezetimibe with rosuvastatin calcium</ActiveIngredient>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/06/2019 16:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>414</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>203688-C01-01-BL600.jpg</ImageFileName>
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							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RSV 40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>203688-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>203689</Austr>
				<PresentationName>Ezalo</PresentationName>
    			<PresentionStrength>10mg/10mg</PresentionStrength>
    			<PresentationForm>Pack</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>composite pack</Container>
    			<TGAIngredient>Ezetimibe,Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Ezalo Composite Pack</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcezalp10821</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ezetimibe with rosuvastatin calcium</ActiveIngredient>
						<ReleaseDate>2021-08-18 14:21:09.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/06/2019 16:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>414</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>203689-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RSV 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>203689-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>203691</Austr>
				<PresentationName>Ezalo</PresentationName>
    			<PresentionStrength>10mg/20mg</PresentionStrength>
    			<PresentationForm>Pack</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>composite pack</Container>
    			<TGAIngredient>Ezetimibe,Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Ezalo Composite Pack</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcezalp10821</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ezetimibe with rosuvastatin calcium</ActiveIngredient>
						<ReleaseDate>2021-08-18 14:21:09.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/06/2019 16:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>414</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>203691-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RSV 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>203691-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>203693</Austr>
				<PresentationName>Ezalo</PresentationName>
    			<PresentionStrength>10mg/5mg</PresentionStrength>
    			<PresentationForm>Pack</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>composite pack</Container>
    			<TGAIngredient>Ezetimibe,Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Ezalo Composite Pack</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcezalp10821</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ezetimibe with rosuvastatin calcium</ActiveIngredient>
						<ReleaseDate>2021-08-18 14:21:09.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/06/2019 16:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>414</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>203693-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RSV 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>203693-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ezemichol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>263224</Austr>
				<PresentationName>Ezemichol</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/10/2018 16:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>263224-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ezetimibe (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>263212</Austr>
				<PresentationName>APO-Ezetimibe</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ezetimibe</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/11/2018 19:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>263212-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ezetimibe/Simvastatin (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>279099</Austr>
				<PresentationName>APO-Ezetimibe/Simvastatin</PresentationName>
    			<PresentionStrength>10mg/20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ezetimibe,Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/11/2018 19:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light tan mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>512</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>279099-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>279116</Austr>
				<PresentationName>APO-Ezetimibe/Simvastatin</PresentationName>
    			<PresentionStrength>10mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin,Ezetimibe</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/11/2018 19:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light tan mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>511</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>279116-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>279121</Austr>
				<PresentationName>APO-Ezetimibe/Simvastatin</PresentationName>
    			<PresentionStrength>10mg/40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ezetimibe,Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/04/2019 18:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light tan mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>513</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>279121-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>279123</Austr>
				<PresentationName>APO-Ezetimibe/Simvastatin</PresentationName>
    			<PresentionStrength>10mg/80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ezetimibe,Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/11/2018 19:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light tan mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>515</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>279123-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ezetrol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>91161</Austr>
				<PresentationName>Ezetrol</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ezetimibe</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Ezetrol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ezetimibe</ActiveIngredient>
						<ReleaseDate>2021-04-16 09:31:54.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/10/2008 19:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>414</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>91161-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ezovir</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>343761</Austr>
				<PresentationName>Ezovir for Genital Herpes</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>famciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Ezovir for Cold Sores (new formulation)</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>famciclovir</ActiveIngredient>
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					</DocumentQualifiers>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Ezovir for shingles (new formulation)</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>famciclovir</ActiveIngredient>
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					</DocumentQualifiers>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Ezovir for genital herpes (new formulation)</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>famciclovir</ActiveIngredient>
						<ReleaseDate>2022-08-30 08:25:01.0</ReleaseDate>
					</DocumentQualifiers>
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				<Images>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/11/2022 16:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>FM</Side1Marking>
							<Side2Marking>250</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>343761-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>343762</Austr>
				<PresentationName>Ezovir for Gential Herpes</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>famciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Ezovir for Cold Sores (new formulation)</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>famciclovir</ActiveIngredient>
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					</DocumentQualifiers>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Ezovir for shingles (new formulation)</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>195174</Austr>
				<PresentationName>Famciclovir AN</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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				<Austr>195175</Austr>
				<PresentationName>Famciclovir AN</PresentationName>
    			<PresentionStrength>125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white to pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>X</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195175-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
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			</Presentations>
			<Presentations>
				<Austr>195181</Austr>
				<PresentationName>Famciclovir AN</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>07/12/2017 13:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>X</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195181-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Famciclovir (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>160556</Austr>
				<PresentationName>APO-Famciclovir</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Famciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>FAM 250</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>160556-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>160559</Austr>
				<PresentationName>APO-Famciclovir</PresentationName>
    			<PresentionStrength>125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Famciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>FAM 125</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
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			<Presentations>
				<Austr>172443</Austr>
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    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Famciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablet</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>FAM500</Side1Marking>
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							<Views>
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			<Presentations>
				<Austr>201911</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Side1Marking>FAM500</Side1Marking>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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							<Shape>round</Shape>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
				<Austr>177012</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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							<DoseForm>Tablets</DoseForm>
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			<Presentations>
				<Austr>157789</Austr>
				<PresentationName>Famciclovir Mylan (formerly Ezovir)</PresentationName>
    			<PresentionStrength>125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Famciclovir</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<QualiferData>genital herpes</QualiferData>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>famciclovir</ActiveIngredient>
						<ReleaseDate>2021-06-28 11:19:43.0</ReleaseDate>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
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			</Presentations>
			<Presentations>
				<Austr>205534</Austr>
				<PresentationName>Famciclovir Mylan Cold Sore Relief (formerly Ezovir)</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>famciclovir</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>famciclovir</ActiveIngredient>
						<ReleaseDate>2021-06-28 11:19:29.0</ReleaseDate>
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						<DateEffective>19/03/2014 10:22</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>FAM 500</Side1Marking>
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		</Brand><Brand>
			<brandname>Famciclovir (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>162313</Austr>
				<PresentationName>Famciclovir Sandoz</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Famciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>FV</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>162313-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>162314</Austr>
				<PresentationName>Famciclovir Sandoz</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Famciclovir</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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						<DateEffective>20/03/2013 11:45</DateEffective>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>FV500</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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		</Brand><Brand>
			<brandname>Famciclovir (SCP)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>176988</Austr>
				<PresentationName>Famciclovir SCP</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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						<DateEffective>03/12/2013 15:49</DateEffective>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>FM</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>176988-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>176990</Austr>
				<PresentationName>Famciclovir SCP</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>20/01/2016 10:10</DateEffective>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>FM</Side1Marking>
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							<Views>
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								<ImageFileName>176990-C01-01-BL600.jpg</ImageFileName>
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		</Brand><Brand>
			<brandname>Famotidine (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>186280</Austr>
				<PresentationName>Famotidine AN</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Scoring>unscored</Scoring>
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			<Presentations>
				<Austr>186281</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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							<DoseForm>Tablets</DoseForm>
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		</Brand><Brand>
			<brandname>Famotidine (GenRx)</brandname>
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			<Presentations>
				<Austr>91513</Austr>
				<PresentationName>GenRx Famotidine</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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		</Brand><Brand>
			<brandname>Famotidine (Sandoz)</brandname>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Famotidine</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
				<Austr>94332</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Famotidine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Views>
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			</Presentations>
		</Brand><Brand>
			<brandname>Famvir</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>201264</Austr>
				<PresentationName>Famvir</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>FV500</Side1Marking>
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							<Views>
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			<Presentations>
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				<PresentationName>Famvir</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Famciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<QualiferData>14, 21</QualiferData>
						<DocumentName>Famvir for Shingles</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
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						</DocumentTypes>
						<ActiveIngredient>famciclovir</ActiveIngredient>
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					<DocumentQualifiers>
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						<QualiferData>20, 56</QualiferData>
						<DocumentName>Famvir for genital herpes</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
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						</DocumentTypes>
						<ActiveIngredient>famciclovir</ActiveIngredient>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
							<Side1Marking>FV</Side1Marking>
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							<Views>
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			<Presentations>
				<Austr>54668</Austr>
				<PresentationName>Famvir</PresentationName>
    			<PresentionStrength>125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Famciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType>Pack Size</QualifierType>
						<QualiferData>40</QualiferData>
						<DocumentName>Famvir for genital herpes</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>iycfamvg10220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>famciclovir</ActiveIngredient>
						<ReleaseDate>2020-04-20 16:52:08.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/12/2008 11:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>FV</Side1Marking>
							<Side2Marking>125</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>54668-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>67391</Austr>
				<PresentationName>Famvir</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Famciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType>Pack Size</QualifierType>
						<QualiferData>30</QualiferData>
						<DocumentName>Famvir for Shingles</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>iycfamvs10220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>famciclovir</ActiveIngredient>
						<ReleaseDate>2020-04-16 15:45:42.0</ReleaseDate>
					</DocumentQualifiers>
					<DocumentQualifiers>
						<QualifierType>Pack Size</QualifierType>
						<QualiferData>56</QualiferData>
						<DocumentName>Famvir for genital herpes</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>iycfamvg10220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>famciclovir</ActiveIngredient>
						<ReleaseDate>2020-04-20 16:52:08.0</ReleaseDate>
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					<Versions>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>03/12/2008 11:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>FV 500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>67391-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fareston</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>59743</Austr>
				<PresentationName>Fareston</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Toremifene citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/10/2010 11:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to almost white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TO 60</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>59743-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Faverin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>64388</Austr>
				<PresentationName>Faverin</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
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						<DateEffective>14/05/2018 16:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>313 313</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>64388-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>90057</Austr>
				<PresentationName>Faverin</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/05/2018 16:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>291 291</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>90057-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Favic</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>159602</Austr>
				<PresentationName>Favic</PresentationName>
    			<PresentionStrength>125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>FC 125</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159602-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>159611</Austr>
				<PresentationName>Favic</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>14/05/2018 16:09</DateEffective>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>FC 250</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159611-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>159619</Austr>
				<PresentationName>Favic</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/05/2018 16:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>FC 500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159619-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Febridol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>287227</Austr>
				<PresentationName>Febridol</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/03/2019 15:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>287227-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>287227-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Feldene</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>37312</Austr>
				<PresentationName>Feldene-D</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Piroxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Feldene and Feldene-D</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>piroxicam</ActiveIngredient>
						<ReleaseDate>2022-01-17 09:33:54.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/08/2008 10:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>FEL 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>37312-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>47654</Austr>
				<PresentationName>Feldene</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Piroxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Feldene and Feldene-D</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>piroxicam</ActiveIngredient>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>28/08/2008 10:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>maroon</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Pfizer</Side1Marking>
							<Side2Marking>FEL20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>47654-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>47656</Austr>
				<PresentationName>Feldene</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Piroxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Feldene and Feldene-D</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>piroxicam</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue/maroon</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Pfizer</Side1Marking>
							<Side2Marking>FEL10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>47656-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Felodil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>128793</Austr>
				<PresentationName>Felodil XR</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>128793-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>128795</Austr>
				<PresentationName>Felodil XR</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish-brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			<brandname>Felodur</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>60980</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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			</Presentations>
			<Presentations>
				<Austr>60981</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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							<View>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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							<Views>
							<View>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
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			<brandname>Femara</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>60605</Austr>
				<PresentationName>Femara</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Letrozole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<DocumentQualifiers>
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						<QualiferData></QualiferData>
						<DocumentName>Femara</DocumentName>
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								<Format>PDF</Format>
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							<PhaseItem>1</PhaseItem>
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							<Side1Marking>FV</Side1Marking>
							<Side2Marking>CG</Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>60605-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Femme-Tab ED</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>170388</Austr>
				<PresentationName>Femme-Tab ED</PresentationName>
    			<PresentionStrength>30mcg/150mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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				<Images>
					<Versions>
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							<PhaseItem>1</PhaseItem>
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							<View>
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							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<View>
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			</Presentations>
			<Presentations>
				<Austr>170389</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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					<Versions>
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							<PhaseItem>1</PhaseItem>
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							<Side2Marking></Side2Marking>
							<Views>
							<View>
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							<DoseForm>Tablets</DoseForm>
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							<Side2Marking></Side2Marking>
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							<View>
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			</Presentations>
		</Brand><Brand>
			<brandname>Femolet</brandname>
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			<Presentations>
				<Austr>166010</Austr>
				<PresentationName>Femolet</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Letrozole</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Femolet</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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							<Side1Marking>LZ 2.5</Side1Marking>
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			<brandname>Femoston</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>219882</Austr>
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    			<PresentionStrength>1mg+1mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Dydrogesterone,Oestradiol</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
							<Side1Marking>379</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>219882-C02-01-BL600.jpg</ImageFileName>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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							<DoseForm>Tablets</DoseForm>
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							<Side1Marking>379</Side1Marking>
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							<Views>
							<View>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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		</Brand><Brand>
			<brandname>Femzole</brandname>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
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							<View>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>170209-C01-01-BL600.jpg</ImageFileName>
							</View>
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						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fenac</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>165706</Austr>
				<PresentationName>Fenac</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Diclofenac sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Fenac</DocumentName>
						<DocumentTypes>
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								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>diclofenac sodium</ActiveIngredient>
						<ReleaseDate>2022-01-17 08:11:34.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>21/10/2010 16:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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								<ImageFileName>165706-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>165707</Austr>
				<PresentationName>Fenac</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Diclofenac sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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								<Format>PDF</Format>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fendex</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>184621</Austr>
				<PresentationName>Fendex ER</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Felodipine</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>F5</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184621-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>184622</Austr>
				<PresentationName>Fendex ER</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Felodipine</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>F10</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			<Presentations>
				<Austr>184623</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Felodipine</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateEffective>19/03/2014 10:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>F2</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184623-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Fenezal</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>134531</Austr>
				<PresentationName>Sandoz Fenezal</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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							<Shape>round</Shape>
							<Side1Marking>PN 10</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>134532</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PN 25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>134532-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fenocol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>288060</Austr>
				<PresentationName>Fenocol</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/02/2020 16:59</DateEffective>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>458</Side1Marking>
							<Side2Marking>Cipla</Side2Marking>
							<Views>
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			</Presentations>
		</Brand><Brand>
			<brandname>Fenofibrate (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>291652</Austr>
				<PresentationName>APO-Fenofibrate</PresentationName>
    			<PresentionStrength>145mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Shape>oblong</Shape>
							<Side1Marking>F</Side1Marking>
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							<Views>
							<View>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fenofibrate (Viatris)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>230443</Austr>
				<PresentationName>Fenofibrate Viatris</PresentationName>
    			<PresentionStrength>145mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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			<brandname>Fentora</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>218433</Austr>
				<PresentationName>Fentora</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient>Fentanyl citrate</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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						<DocumentName>Fentora</DocumentName>
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						<ActiveIngredient>fentanyl citrate</ActiveIngredient>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<ReleaseDate>2021-08-18 16:55:56.0</ReleaseDate>
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						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>1</Side1Marking>
							<Side2Marking>C</Side2Marking>
							<Views>
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								<ViewLabel>C</ViewLabel>
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							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>218436</Austr>
				<PresentationName>Fentora</PresentationName>
    			<PresentionStrength>800mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fentanyl citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Fentora</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcfento10821</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fentanyl citrate</ActiveIngredient>
						<ReleaseDate>2021-08-18 16:55:56.0</ReleaseDate>
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				</Documents>
				<Images>
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						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>8</Side1Marking>
							<Side2Marking>C</Side2Marking>
							<Views>
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								<ViewLabel>C</ViewLabel>
								<ImageFileName>218436-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>218437</Austr>
				<PresentationName>Fentora</PresentationName>
    			<PresentionStrength>200mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fentanyl citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Fentora</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcfento10821</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fentanyl citrate</ActiveIngredient>
						<ReleaseDate>2021-08-18 16:55:56.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>2</Side1Marking>
							<Side2Marking>C</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>218437-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ferriprox</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>280204</Austr>
				<PresentationName>Ferriprox</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Deferiprone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/04/2020 09:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>APO 1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>280204-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>93946</Austr>
				<PresentationName>Ferriprox</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Deferiprone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/11/2017 11:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>APO 500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>93946-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ferro-f</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>128099</Austr>
				<PresentationName>Ferro-f-tab</PresentationName>
    			<PresentionStrength>310mg/350mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/09/2010 14:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>sandy brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>128099-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ferro-Grad C</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>66841</Austr>
				<PresentationName>Ferro-Grad C</PresentationName>
    			<PresentionStrength>325mg/562.4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/07/2019 13:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>66841-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ferro-Grad F</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>77937</Austr>
				<PresentationName>Ferro-Grad F</PresentationName>
    			<PresentionStrength>250mg/300mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/07/2019 13:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>speckled grey-tan and pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>M</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>77937-C01-02-BL600.jpg</ImageFileName>
							</View>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ferro-Gradumet</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>59522</Austr>
				<PresentationName>Ferro-Gradumet</PresentationName>
    			<PresentionStrength>325mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/11/2008 10:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Abbott logo</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>59522-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ferro-tab</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>175706</Austr>
				<PresentationName>Ferro-tab</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2011 13:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>175706-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fexal</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>140284</Austr>
				<PresentationName>Fexal</PresentationName>
    			<PresentionStrength>120mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>012</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>140284-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>140285</Austr>
				<PresentationName>Fexal</PresentationName>
    			<PresentionStrength>180mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>018</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>140285-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fexofenadine (Apohealth)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>232034</Austr>
				<PresentationName>Apohealth Fexofenadine Hayfever &amp; Allergy Relief</PresentationName>
    			<PresentionStrength>180mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/02/2017 12:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>FXF</Side1Marking>
							<Side2Marking>180</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>232034-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fexofenadine (Generic Health)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>186664</Austr>
				<PresentationName>Fexorelief</PresentationName>
    			<PresentionStrength>120mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/05/2017 14:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>FXF</Side1Marking>
							<Side2Marking>120</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>186664-C01-02-BL600.jpg</ImageFileName>
							</View>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>233592</Austr>
				<PresentationName>Fexorelief</PresentationName>
    			<PresentionStrength>180mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/05/2017 17:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>caplet-shaped</Shape>
							<Side1Marking>180</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>233592-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fexotabs</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>98161</Austr>
				<PresentationName>Fexotabs</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
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			</Presentations>
			<Presentations>
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				<PresentationName>Fexotabs</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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				</Images>
			</Presentations>
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			<brandname>Fibsol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>101316</Austr>
				<PresentationName>Fibsol</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
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							<Side2Marking></Side2Marking>
							<Views>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101317</Austr>
				<PresentationName>Fibsol</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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							<DoseForm>Tablets</DoseForm>
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							<Side2Marking></Side2Marking>
							<Views>
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			</Presentations>
			<Presentations>
				<Austr>101318</Austr>
				<PresentationName>Fibsol</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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							<DoseForm>Tablets</DoseForm>
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			<Presentations>
				<Austr>189653</Austr>
				<PresentationName>Finapen</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Views>
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			</Presentations>
		</Brand><Brand>
			<brandname>Finasta</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>127409</Austr>
				<PresentationName>Finasta</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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							<DoseForm>Tablets</DoseForm>
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							<Side2Marking></Side2Marking>
							<Views>
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			</Presentations>
		</Brand><Brand>
			<brandname>Finasteride (Alphapharm)</brandname>
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			<Presentations>
				<Austr>186305</Austr>
				<PresentationName>Finasteride Alphapharm</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Finasteride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>151</Side1Marking>
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		</Brand><Brand>
			<brandname>Finasteride (Amneal)</brandname>
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			<Presentations>
				<Austr>189272</Austr>
				<PresentationName>Finasteride AN</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Scoring>unscored</Scoring>
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							<Views>
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			</Presentations>
			<Presentations>
				<Austr>189273</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
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		</Brand><Brand>
			<brandname>Finasteride (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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							<Views>
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			<brandname>Finasteride (Generic Health)</brandname>
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   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>18/10/2010 15:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>F5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>155235-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Finide</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>161631</Austr>
				<PresentationName>Finide</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Finasteride</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<QualiferData></QualiferData>
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						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>finasteride</ActiveIngredient>
						<ReleaseDate>2019-08-16 15:13:03.0</ReleaseDate>
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				</Documents>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/12/2018 10:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>FIN</Side1Marking>
							<Side2Marking>5</Side2Marking>
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								<ViewLabel>C</ViewLabel>
								<ImageFileName>161631-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Finnacar</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>143402</Austr>
				<PresentationName>Finnacar</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>14/05/2018 16:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rounded triangle</Shape>
							<Side1Marking>RG</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>143402-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Flagyl</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>160171</Austr>
				<PresentationName>Flagyl</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metronidazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<QualiferData></QualiferData>
						<DocumentName>Flagyl</DocumentName>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>metronidazole</ActiveIngredient>
						<ReleaseDate>2022-03-29 15:56:19.0</ReleaseDate>
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				<Images>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2010 15:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>MTZ 200</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>160171-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>160174</Austr>
				<PresentationName>Flagyl</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metronidazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2010 15:30</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>MTZ 400</Side1Marking>
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							<Views>
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								<ViewLabel>A</ViewLabel>
								<ImageFileName>160174-A01-01-BL600.jpg</ImageFileName>
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								<ViewLabel>B</ViewLabel>
    							<ImageFileName>160174-B01-01-BL600.jpg</ImageFileName>
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			</Presentations>
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			<brandname>Flecainide (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>289980</Austr>
				<PresentationName>APO-Flecainide</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>flecainide acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/03/2020 20:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>F1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>289980-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Flecainide acetate (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>232473</Austr>
				<PresentationName>Flecainide Sandoz</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/01/2018 11:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>FI</Side1Marking>
							<Side2Marking>C</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>232473-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>232474</Austr>
				<PresentationName>Flecainide Sandoz</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/01/2018 11:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C FJ</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>232474-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Flecatab</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>344750</Austr>
				<PresentationName>Flecatab</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>flecainide acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Flecatab</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>flecainide acetate</ActiveIngredient>
						<ReleaseDate>2022-04-08 11:26:36.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/11/2022 16:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>FC 50</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>344750-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>68651</Austr>
				<PresentationName>Flecatab</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Flecainide acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Flecatab</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>flecainide acetate</ActiveIngredient>
						<ReleaseDate>2022-04-08 11:26:36.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>FC 100</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>68651-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Flomaxtra</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>115534</Austr>
				<PresentationName>Flomaxtra</PresentationName>
    			<PresentionStrength>400mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tamsulosin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Flomaxtra</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tamsulosin hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-07-22 11:36:58.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/08/2008 10:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>04</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>115534-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Flopen</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>209367</Austr>
				<PresentationName>Flopen</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>flucloxacillin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Flopen</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>flucloxacillin sodium monohydrate</ActiveIngredient>
						<ReleaseDate>2020-06-24 14:42:22.0</ReleaseDate>
					</DocumentQualifiers>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>18/11/2021 11:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>F250</Side1Marking>
							<Side2Marking>F250</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>209367-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>209368</Austr>
				<PresentationName>Flopen</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>flucloxacillin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Flopen</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>flucloxacillin sodium monohydrate</ActiveIngredient>
						<ReleaseDate>2020-06-24 14:42:22.0</ReleaseDate>
					</DocumentQualifiers>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>18/11/2021 11:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>F500</Side1Marking>
							<Side2Marking>F500</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>209368-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Flucloxacillin (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>226374</Austr>
				<PresentationName>APO-Flucloxacillin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Flucloxacillin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>F 500</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>226374-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>226382</Austr>
				<PresentationName>APO-Flucloxacillin</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Flucloxacillin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>F 250</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>226382-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fluconazole (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167038</Austr>
				<PresentationName>Fluconazole AN</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167038-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fluconazole (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>151630</Austr>
				<PresentationName>Apo-Fluconazole</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/02/2010 10:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>violet and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151630-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>152959</Austr>
				<PresentationName>Apo-Fluconazole One</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>fluconazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 12:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>sky blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152959-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>293315</Austr>
				<PresentationName>Fluconazole Apotex</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluconazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/04/2019 18:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>purple and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>293315-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fluconazole (Generic Health)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>170239</Austr>
				<PresentationName>Pharmacy Action Femrelief One</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>170239-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fluconazole (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>104285</Austr>
				<PresentationName>Fluconazole Sandoz</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluconazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>turquoise and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>FC 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>104285-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>104288</Austr>
				<PresentationName>Fluconazole Sandoz</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluconazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>FC 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>104288-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>104293</Austr>
				<PresentationName>Fluconazole Sandoz</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluconazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>purple and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>FC 200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>104293-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fludara</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>81998</Austr>
				<PresentationName>Fludara</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fludarabine phosphate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Fludara Oral</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcfluda10420</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fludarabine phosphate</ActiveIngredient>
						<ReleaseDate>2020-04-30 14:19:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/05/2021 08:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>salmon</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LN hexagon</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>81998-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Flufeme</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>132827</Austr>
				<PresentationName>Flufeme</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>FC 150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>132827-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fluotex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>273925</Austr>
				<PresentationName>Fluotex</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/10/2018 16:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green and off-white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>FLX</Side1Marking>
							<Side2Marking>MIL</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>273925-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fluoxetine (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>148137</Austr>
				<PresentationName>Fluoxetine AN</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque light green and opaque ivory</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>148137-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fluoxetine (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>160765</Austr>
				<PresentationName>APO-Fluoxetine</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/11/2017 11:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque light green and opaque ivory</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>160765-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>273924</Austr>
				<PresentationName>Fluoxetine Apotex</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>fluoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2022 11:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green and off-white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>FLX</Side1Marking>
							<Side2Marking>MIL</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
		</Brand><Brand>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>92687</Austr>
				<PresentationName>Fluoxetine-AS</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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						<DateEffective>23/02/2009 12:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light green and ivory</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fluoxetine (Blooms the Chemist)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>73882</Austr>
				<PresentationName>Blooms the Chemist Fluoxetine</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>fluoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/07/2008 10:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green and ivory</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73882-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fluoxetine (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>73880</Austr>
				<PresentationName>Chemmart Fluoxetine</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/07/2008 10:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green and ivory</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73880-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fluoxetine (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>146600</Austr>
				<PresentationName>Fluoxetine generichealth</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light green and off-white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>146600-C01-02-BL600.jpg</ImageFileName>
							</View>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fluoxetine (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>130619</Austr>
				<PresentationName>Pharmacor Fluoxetine</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/08/2009 12:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Capsules</DoseForm>
							<Colour>green and ivory</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
					</Versions>
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			</Presentations>
		</Brand><Brand>
			<brandname>Fluoxetine (Ranbaxy)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>146606</Austr>
				<PresentationName>Fluoxetine RBX</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/09/2013 17:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green and off-white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fluoxetine (Sandoz)</brandname>
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			<Presentations>
				<Austr>64564</Austr>
				<PresentationName>Fluoxetine Sandoz</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/09/2008 17:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
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							<Views>
							<View>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fluoxetine (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>73879</Austr>
				<PresentationName>Terry White Chemists Fluoxetine</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green and ivory</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Flutamin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>65675</Austr>
				<PresentationName>Flutamin</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Flutamide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Flutamin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>flutamide</ActiveIngredient>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>FT 250</Side1Marking>
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							<Views>
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							<View>
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							</Views>
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			</Presentations>
		</Brand><Brand>
			<brandname>Fluvoxamine (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>147380</Austr>
				<PresentationName>Apo-Fluvoxamine</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluvoxamine maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>golden</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>F 50</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>147389</Austr>
				<PresentationName>Apo-Fluvoxamine</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluvoxamine maleate</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
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							<Side1Marking>FLU 100</Side1Marking>
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							<Views>
							<View>
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			<brandname>Fluvoxamine (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>168717</Austr>
				<PresentationName>Fluvoxamine-GA</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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							<DoseForm>Tablets</DoseForm>
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			</Presentations>
			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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							<Side1Marking>313 313</Side1Marking>
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							<Views>
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			<brandname>Fluzole</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>120778</Austr>
				<PresentationName>Fluzole</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<PresentationName>Fonat</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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			<brandname>Fonat Plus</brandname>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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			<Presentations>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/09/2008 10:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified rectangle-shaped</Shape>
							<Side1Marking>270</Side1Marking>
							<Side2Marking>bone image</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>136846-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fosetic</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>143587</Austr>
				<PresentationName>Fosetic</PresentationName>
    			<PresentionStrength>20mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2011 12:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>FH</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>143587-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fosinopril Sodium (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>119874</Austr>
				<PresentationName>APO-Fosinopril</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fosinopril sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/09/2014 10:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shape with indents</Shape>
							<Side1Marking>FOS-10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>119874-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>119876</Austr>
				<PresentationName>APO-Fosinopril</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fosinopril sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/09/2014 10:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>FOS-20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>119876-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fosinopril Sodium/HCT (Actavis)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>212128</Austr>
				<PresentationName>Fosinopril/HCT Actavis</PresentationName>
    			<PresentionStrength>20mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 14:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>FH</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>212128-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fosinopril Sodium/HCTZ (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>223503</Austr>
				<PresentationName>APO-Fosinopril HCTZ</PresentationName>
    			<PresentionStrength>20mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-24 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>FH</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>223503-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fosinopril/HCTZ (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>151949</Austr>
				<PresentationName>Fosinopril/HCTZ-GA</PresentationName>
    			<PresentionStrength>10mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 10:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>RC 3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151949-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fosipril</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>100059</Austr>
				<PresentationName>Fosipril</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>FI 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>100059-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>100060</Austr>
				<PresentationName>Fosipril</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>FI 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>100060-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Fosrenol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>106960</Austr>
				<PresentationName>Fosrenol</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Lanthanum carbonate hydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Fosrenol Chewable Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
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								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lanthanum carbonate hydrate</ActiveIngredient>
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				<Images>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/09/2015 09:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>S405 500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>106960-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>106960-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>106962</Austr>
				<PresentationName>Fosrenol</PresentationName>
    			<PresentionStrength>750mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Lanthanum carbonate hydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Fosrenol Chewable Tablets</DocumentName>
						<DocumentTypes>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lanthanum carbonate hydrate</ActiveIngredient>
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						<DateEffective>25/09/2015 09:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>S405 750</Side1Marking>
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								<ViewLabel>B</ViewLabel>
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							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>106964</Austr>
				<PresentationName>Fosrenol</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Lanthanum carbonate hydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<QualiferData></QualiferData>
						<DocumentName>Fosrenol Chewable Tablets</DocumentName>
						<DocumentTypes>
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							</AvailableFormats>
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						<ActiveIngredient>lanthanum carbonate hydrate</ActiveIngredient>
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				<Images>
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						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>S405 1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>106964-A01-01-BL600.jpg</ImageFileName>
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							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>106964-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Frakas</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>98653</Austr>
				<PresentationName>Frakas</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/05/2018 16:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dull yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>98653-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Frisium</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>12400</Austr>
				<PresentationName>Frisium</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clobazam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Frisium</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clobazam</ActiveIngredient>
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				<Images>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/07/2008 10:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>B GL</Side1Marking>
							<Side2Marking>logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>12400-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Frusemide (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>186516</Austr>
				<PresentationName>APO-Frusemide</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
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   				<WithdrawalDate></WithdrawalDate>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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			<brandname>Frusemide (Sandoz)</brandname>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/07/2014 15:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>215</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204501-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gabapentin (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>156104</Austr>
				<PresentationName>Gabapentin AN</PresentationName>
    			<PresentionStrength>800mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/12/2017 13:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156104-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156105</Austr>
				<PresentationName>Gabapentin AN</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/12/2017 13:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156105-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gabapentin (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>131464</Austr>
				<PresentationName>APO-Gabapentin</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-09-20 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/09/2018 09:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>GAB 600</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>131464-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>151318</Austr>
				<PresentationName>APO-Gabapentin</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-09-20 00:00:00'}</WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/05/2010 10:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>112</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151318-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>306886</Austr>
				<PresentationName>Gabapentin Apotex</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/03/2020 22:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>306886-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>306887</Austr>
				<PresentationName>Gabapentin Apotex</PresentationName>
    			<PresentionStrength>800mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/03/2020 22:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>306887-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>81776</Austr>
				<PresentationName>APO-Gabapentin</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-09-20 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/08/2008 09:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white opaque and yellow opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>113</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>81776-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>81777</Austr>
				<PresentationName>APO-Gabapentin</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-09-20 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/08/2008 09:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white opaque and orange opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>114</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>81777-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gabapentin (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>81811</Austr>
				<PresentationName>Gabapentin-GA</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 12:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>113</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>81811-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>81812</Austr>
				<PresentationName>Gabapentin-GA</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 12:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>114</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>81812-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gabapentin (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>219922</Austr>
				<PresentationName>Gabapentin GH</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/05/2017 14:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>brown</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>219922-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>219923</Austr>
				<PresentationName>Gabapentin GH</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/05/2017 14:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>219923-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gabapentin (Pfizer)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>80334</Austr>
				<PresentationName>Gabapentin Pfizer</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/02/2013 15:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>G</Side1Marking>
							<Side2Marking>5026</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>80334-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>80335</Austr>
				<PresentationName>Gabapentin Pfizer</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/02/2013 15:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>G</Side1Marking>
							<Side2Marking>5027</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>80335-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>80336</Austr>
				<PresentationName>Gabapentin Pfizer</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/02/2013 15:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>G</Side1Marking>
							<Side2Marking>5028</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>80336-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>80337</Austr>
				<PresentationName>Gabapentin Pfizer</PresentationName>
    			<PresentionStrength>800mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/12/2010 11:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>NT 26</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>80337-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gabapentin (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>130624</Austr>
				<PresentationName>Pharmacor Gabapentin</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/06/2011 11:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque yellow and opaque white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>113</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>130624-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>130625</Austr>
				<PresentationName>Pharmacor Gabapentin</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/06/2011 11:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white and orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>114</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>130625-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156107</Austr>
				<PresentationName>Pharmacor Gabapentin</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/06/2011 11:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156107-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156108</Austr>
				<PresentationName>Pharmacor Gabapentin</PresentationName>
    			<PresentionStrength>800mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/06/2011 11:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156108-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gabapentin (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>157195</Austr>
				<PresentationName>Gabapentin Sandoz</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>brown</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157195-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>157197</Austr>
				<PresentationName>Gabapentin Sandoz</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157197-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gabaran</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>121833</Austr>
				<PresentationName>Gabaran</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/02/2009 11:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>G 600</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121833-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121843</Austr>
				<PresentationName>Gabaran</PresentationName>
    			<PresentionStrength>800mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/02/2009 11:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>G 800</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121843-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gabitril</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>120271</Austr>
				<PresentationName>Gabitril</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>tiagabine hydrochloride monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Gabitril</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcgabit10218</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tiagabine hydrochloride monohydrate</ActiveIngredient>
						<ReleaseDate>2018-06-06 10:52:00.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/06/2012 13:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>251</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>120271-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>120272</Austr>
				<PresentationName>Gabitril</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>tiagabine hydrochloride monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Gabitril</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcgabit10218</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tiagabine hydrochloride monohydrate</ActiveIngredient>
						<ReleaseDate>2018-06-06 10:52:00.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/06/2012 13:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>252</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>120272-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>120273</Austr>
				<PresentationName>Gabitril</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>tiagabine hydrochloride monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Gabitril</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcgabit10218</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tiagabine hydrochloride monohydrate</ActiveIngredient>
						<ReleaseDate>2018-06-06 10:52:00.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>253</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>120273-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Galantamine (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>182032</Austr>
				<PresentationName>Galantamine AN SR</PresentationName>
    			<PresentionStrength>16mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>flesh opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>182032-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>182036</Austr>
				<PresentationName>Galantamine AN SR</PresentationName>
    			<PresentionStrength>24mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>182036-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>182042</Austr>
				<PresentationName>Galantamine AN SR</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>182042-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Galantamine (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>182030</Austr>
				<PresentationName>APO-Galantamine</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Galantamine hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/03/2013 11:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>182030-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>182034</Austr>
				<PresentationName>APO-Galantamine</PresentationName>
    			<PresentionStrength>24mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Galantamine hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/03/2013 11:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>182034-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>182041</Austr>
				<PresentationName>APO-Galantamine</PresentationName>
    			<PresentionStrength>16mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Galantamine hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/03/2013 11:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>flesh opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>182041-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Galantyl</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>157932</Austr>
				<PresentationName>Galantyl</PresentationName>
    			<PresentionStrength>16mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Galantamine hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Galantyl</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcgalan10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>galantamine hydrobromide</ActiveIngredient>
						<ReleaseDate>2022-07-01 17:18:36.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/04/2011 14:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>pale pink and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>MYLAN GT 16</Side1Marking>
							<Side2Marking>MYLAN GT 16</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157932-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>157933</Austr>
				<PresentationName>Galantyl</PresentationName>
    			<PresentionStrength>24mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Galantamine hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Galantyl</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcgalan10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>galantamine hydrobromide</ActiveIngredient>
						<ReleaseDate>2022-07-01 17:18:36.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/04/2011 14:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>pink and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>MYLAN GT 24</Side1Marking>
							<Side2Marking>MYLAN GT 24</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157933-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>157934</Austr>
				<PresentationName>Galantyl</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Galantamine hydrobromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Galantyl</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcgalan10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>galantamine hydrobromide</ActiveIngredient>
						<ReleaseDate>2022-07-01 17:18:36.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/04/2011 14:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>pink and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>MYLAN GT 8</Side1Marking>
							<Side2Marking>MYLAN GT 8</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157934-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Galvumet</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>161216</Austr>
				<PresentationName>Galvumet</PresentationName>
    			<PresentionStrength>50mg/500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Metformin hydrochloride,Vildagliptin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Galvumet</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcgamor10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>vildagliptin with metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-07-25 17:21:38.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/07/2011 12:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LLO</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>161216-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>161217</Austr>
				<PresentationName>Galvumet</PresentationName>
    			<PresentionStrength>50mg/850mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Vildagliptin,Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Galvumet</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcgamor10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>vildagliptin with metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-07-25 17:21:38.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/03/2011 13:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SEH</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>161217-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>161218</Austr>
				<PresentationName>Galvumet</PresentationName>
    			<PresentionStrength>50mg/1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Vildagliptin,Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Galvumet</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcgamor10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>vildagliptin with metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-07-25 17:21:38.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/03/2011 13:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>FLO</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>161218-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Galvus</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>159561</Austr>
				<PresentationName>Galvus</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Vildagliptin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Galvus</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcgalor10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>vildagliptin</ActiveIngredient>
						<ReleaseDate>2022-08-02 10:18:41.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/01/2011 13:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to light yellowish</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>FB</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159561-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gamine XR</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>182028</Austr>
				<PresentationName>Gamine XR</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/04/2018 13:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>182028-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>182038</Austr>
				<PresentationName>Gamine XR</PresentationName>
    			<PresentionStrength>16mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/04/2018 13:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>flesh opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>182038-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>182040</Austr>
				<PresentationName>Gamine XR</PresentationName>
    			<PresentionStrength>24mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/04/2018 13:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>182040-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gantin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>78624</Austr>
				<PresentationName>Gantin</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/09/2011 15:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>78624-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>78625</Austr>
				<PresentationName>Gantin</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/09/2011 15:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>78625-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>78626</Austr>
				<PresentationName>Gantin</PresentationName>
    			<PresentionStrength>800mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/09/2011 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>NT 26</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>78626-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gapentin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>107472</Austr>
				<PresentationName>Gapentin</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/05/2018 16:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>G 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>107472-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>107494</Austr>
				<PresentationName>Gapentin</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/05/2018 16:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>G 300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>107494-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>107498</Austr>
				<PresentationName>Gapentin</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/05/2018 16:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>G 400</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>107498-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156106</Austr>
				<PresentationName>Gapentin</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/05/2018 16:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156106-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gastrex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>196267</Austr>
				<PresentationName>Gastrex</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/12/2012 10:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>grey and green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>196267-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gastro-Soothe</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>205028</Austr>
				<PresentationName>Gastro-Soothe</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/09/2013 14:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>205028-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gastro-Stop</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>48935</Austr>
				<PresentationName>Gastro-Stop</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/11/2008 13:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green and grey</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>LOP 2</Side1Marking>
							<Side2Marking>LOP 2</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>48935-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gaviscon</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>133124</Austr>
				<PresentationName>Gaviscon Cool Mint</PresentationName>
    			<PresentionStrength>250mg/133.5mg/80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/03/2011 10:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light grey</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>GC 250</Side1Marking>
							<Side2Marking>sword</Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>133124-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>133124-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156038</Austr>
				<PresentationName>Gaviscon Lemon</PresentationName>
    			<PresentionStrength>250mg/133.5mg/80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/05/2011 11:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>G 250</Side1Marking>
							<Side2Marking>sword</Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>156038-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>156038-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156041</Austr>
				<PresentationName>Gaviscon Peppermint</PresentationName>
    			<PresentionStrength>250mg/133.5mg/80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/05/2011 11:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>G 250</Side1Marking>
							<Side2Marking>sword</Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>156041-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>156041-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gemfibrozil (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>73848</Austr>
				<PresentationName>Chemmart Gemfibrozil</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Gemfibrozil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/05/2012 09:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>APO 034</Side1Marking>
							<Side2Marking>600</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73848-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gemfibrozil (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>147595</Austr>
				<PresentationName>Gemfibrozil-GA</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 10:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>600</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>147595-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gemfibrozil (GenRx)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>73850</Austr>
				<PresentationName>GenRx Gemfibrozil</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Gemfibrozil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/05/2012 10:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>APO 034</Side1Marking>
							<Side2Marking>600</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73850-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gemfibrozil (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>73847</Austr>
				<PresentationName>Terry White Chemists Gemfibrozil</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Gemfibrozil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/05/2012 10:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>APO 034</Side1Marking>
							<Side2Marking>600</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73847-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gemhexal</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>62537</Austr>
				<PresentationName>Gemhexal</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Gemfibrozil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 14:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62537-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>64873</Austr>
				<PresentationName>Gemhexal</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gemfibrozil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 12:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>64873-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Genox</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>40063</Austr>
				<PresentationName>Genox</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tamoxifen citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Genox</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcgenox11221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tamoxifen citrate</ActiveIngredient>
						<ReleaseDate>2021-12-15 13:11:21.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TN 10</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>40063-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>40065</Austr>
				<PresentationName>Genox</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tamoxifen citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Genox</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcgenox11221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tamoxifen citrate</ActiveIngredient>
						<ReleaseDate>2021-12-15 13:11:21.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TN 20</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>40065-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gilenya</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>169890</Austr>
				<PresentationName>Gilenya</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fingolimod hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Gilenya</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcgilor10221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fingolimod</ActiveIngredient>
						<ReleaseDate>2021-02-18 16:38:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/07/2011 12:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>bright yellow opaque and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>FTY 0.5mg</Side1Marking>
							<Side2Marking>two radial bands</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>169890-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>300029</Austr>
				<PresentationName>Gilenya</PresentationName>
    			<PresentionStrength>0.25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>fingolimod hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Gilenya</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcgilor10221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fingolimod</ActiveIngredient>
						<ReleaseDate>2021-02-18 16:38:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>18/09/2019 16:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>ivory opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>FTY 0.25 mg</Side1Marking>
							<Side2Marking>radial band</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>300029-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Giotrif</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>201314</Austr>
				<PresentationName>Giotrif</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>afatinib dimaleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Giotrif</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>bycgiotr10619</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>afatinib dimaleate</ActiveIngredient>
						<ReleaseDate>2019-06-21 12:10:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/07/2014 12:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to slightly yellowish</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>T20</Side1Marking>
							<Side2Marking>Company logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>201314-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>201315</Austr>
				<PresentationName>Giotrif</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>afatinib dimaleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Giotrif</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>bycgiotr10619</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>afatinib dimaleate</ActiveIngredient>
						<ReleaseDate>2019-06-21 12:10:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/07/2014 12:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>T40</Side1Marking>
							<Side2Marking>Company logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>201315-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>201318</Austr>
				<PresentationName>Giotrif</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>afatinib dimaleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Giotrif</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>bycgiotr10619</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>afatinib dimaleate</ActiveIngredient>
						<ReleaseDate>2019-06-21 12:10:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/07/2014 12:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>T30</Side1Marking>
							<Side2Marking>Company logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>201318-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>201320</Austr>
				<PresentationName>Giotrif</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>afatinib dimaleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Giotrif</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>bycgiotr10619</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>afatinib dimaleate</ActiveIngredient>
						<ReleaseDate>2019-06-21 12:10:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/07/2014 12:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>T50</Side1Marking>
							<Side2Marking>Company logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>201320-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gliclazide (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>151303</Austr>
				<PresentationName>Apo-Gliclazide MR</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gliclazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/05/2010 10:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>APO 30</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151303-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>80084</Austr>
				<PresentationName>APO-Gliclazide</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gliclazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/08/2008 09:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>APO 80</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>80084-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Glimepiride (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>156398</Austr>
				<PresentationName>Glimepiride AN</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
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							<Views>
							<View>
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							</Views>
						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>156401</Austr>
				<PresentationName>Glimepiride AN</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
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							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>G4 G4</Side1Marking>
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								<ImageFileName>151573-C01-01-BL600.jpg</ImageFileName>
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			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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							<DoseForm>Tablets</DoseForm>
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    			<Container>blister pack</Container>
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			<Presentations>
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			<Presentations>
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			<Presentations>
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			<Presentations>
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			<Presentations>
				<Austr>156402</Austr>
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			<Presentations>
				<Austr>156404</Austr>
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							<Side1Marking></Side1Marking>
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			</Presentations>
			<Presentations>
				<Austr>156406</Austr>
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							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Glimepiride (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>121781</Austr>
				<PresentationName>Glimepiride Sandoz</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Glimepiride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 16:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light red</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>G 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121781-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121786</Austr>
				<PresentationName>Glimepiride Sandoz</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Glimepiride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 16:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light green</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>G 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121786-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121788</Austr>
				<PresentationName>Glimepiride Sandoz</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Glimepiride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 16:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>G 3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121788-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121790</Austr>
				<PresentationName>Glimepiride Sandoz</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Glimepiride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 16:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>G 4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121790-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Glivec</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>94216</Austr>
				<PresentationName>Glivec Tablets</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Imatinib mesylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Glivec Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcglitb10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>imatinib mesilate</ActiveIngredient>
						<ReleaseDate>2022-08-02 16:32:27.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/12/2008 11:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark yellow to brownish orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>S A</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>94216-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>94217</Austr>
				<PresentationName>Glivec Tablets</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Imatinib mesylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Glivec Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcglitb10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>imatinib mesilate</ActiveIngredient>
						<ReleaseDate>2022-08-02 16:32:27.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/12/2008 11:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark yellow to brownish orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SL SL</Side1Marking>
							<Side2Marking>400</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>94217-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Glucobay</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>43194</Austr>
				<PresentationName>Glucobay</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/04/2010 11:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to yellow-tinged</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>G 50</Side1Marking>
							<Side2Marking>Bayer Cross</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>43194-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>43195</Austr>
				<PresentationName>Glucobay</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/04/2010 11:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to yellow-tinged</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>G 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>43195-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Glucovance</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>96725</Austr>
				<PresentationName>Glucovance</PresentationName>
    			<PresentionStrength>250/1.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Glibenclamide,Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Glucovance</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcgluco10720</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>metformin hydrochloride with glibenclamide</ActiveIngredient>
						<ReleaseDate>2020-07-14 11:00:23.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>250</Side1Marking>
							<Side2Marking>1.25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96725-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>96728</Austr>
				<PresentationName>Glucovance</PresentationName>
    			<PresentionStrength>500/2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Glibenclamide,Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Glucovance</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcgluco10720</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>metformin hydrochloride with glibenclamide</ActiveIngredient>
						<ReleaseDate>2020-07-14 11:00:23.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>2.5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96728-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>96729</Austr>
				<PresentationName>Glucovance</PresentationName>
    			<PresentionStrength>500/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Glibenclamide,Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Glucovance</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcgluco10720</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>metformin hydrochloride with glibenclamide</ActiveIngredient>
						<ReleaseDate>2020-07-14 11:00:23.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96729-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Glyade</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>139728</Austr>
				<PresentationName>Glyade MR</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gliclazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Glyade MR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcglymr10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>gliclazide</ActiveIngredient>
						<ReleaseDate>2022-08-01 15:25:36.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/07/2009 11:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>DIA 30</Side1Marking>
							<Side2Marking>Servier Logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>139728-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>70433</Austr>
				<PresentationName>Glyade</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gliclazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Glyade</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcglyad10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>gliclazide</ActiveIngredient>
						<ReleaseDate>2022-08-01 15:25:09.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>70433-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Glybosay</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>226791</Austr>
				<PresentationName>Glybosay</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/08/2019 16:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ACA 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>226791-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>226792</Austr>
				<PresentationName>Glybosay</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/08/2019 16:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ACA 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>226792-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Glyxambi</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>263556</Austr>
				<PresentationName>Glyxambi</PresentationName>
    			<PresentionStrength>10mg/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>empagliflozin,linagliptin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Glyxambi</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>bycglyxa10922</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>empagliflozin with linagliptan</ActiveIngredient>
						<ReleaseDate>2022-09-21 18:39:28.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/10/2018 11:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>arc triangular</Shape>
							<Side1Marking>10/5</Side1Marking>
							<Side2Marking>Boehringer Ingelheim symbol</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>263556-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>263557</Austr>
				<PresentationName>Glyxambi</PresentationName>
    			<PresentionStrength>25mg/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>empagliflozin,linagliptin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Glyxambi</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>bycglyxa10922</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>empagliflozin with linagliptan</ActiveIngredient>
						<ReleaseDate>2022-09-21 18:39:28.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/10/2018 11:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>arc triangular</Shape>
							<Side1Marking>25/5</Side1Marking>
							<Side2Marking>Boehringer Ingelheim symbol</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>263557-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>GN-Carvedilol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>152437</Austr>
				<PresentationName>GN-Carvedilol</PresentationName>
    			<PresentionStrength>3.125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 11:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CL 3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152437-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>152438</Austr>
				<PresentationName>GN-Carvedilol</PresentationName>
    			<PresentionStrength>6.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 11:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CL 6</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152438-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>152439</Austr>
				<PresentationName>GN-Carvedilol</PresentationName>
    			<PresentionStrength>12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CL 12</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152439-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>152440</Austr>
				<PresentationName>GN-Carvedilol</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 11:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CL 25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152440-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gold Cross Princard</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>178832</Austr>
				<PresentationName>Gold Cross Princard</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/06/2012 15:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>178832-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gold Cross SleepWell</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>171259</Austr>
				<PresentationName>Gold Cross SleepWell</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>doxylamine succinate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/06/2012 15:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>171259-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Gopten</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>45455</Austr>
				<PresentationName>Gopten</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Trandolapril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Gopten</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocgopte10122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>trandolapril</ActiveIngredient>
						<ReleaseDate>2022-01-31 08:23:17.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/11/2008 09:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red and orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>45455-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>45456</Austr>
				<PresentationName>Gopten</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Trandolapril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Gopten</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocgopte10122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>trandolapril</ActiveIngredient>
						<ReleaseDate>2022-01-31 08:23:17.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/11/2008 09:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red and yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>45456-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>45457</Austr>
				<PresentationName>Gopten</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Trandolapril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Gopten</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocgopte10122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>trandolapril</ActiveIngredient>
						<ReleaseDate>2022-01-31 08:23:17.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/11/2008 09:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>45457-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>96969</Austr>
				<PresentationName>Gopten</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Trandolapril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Gopten</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocgopte10122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>trandolapril</ActiveIngredient>
						<ReleaseDate>2022-01-31 08:23:17.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/11/2008 09:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red and maroon</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96969-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Grisovin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>12510</Austr>
				<PresentationName>Grisovin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>124585</Austr>
				<PresentationName>Hyforil</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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			</Presentations>
			<Presentations>
				<Austr>124589</Austr>
				<PresentationName>Hyforil</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
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							<Side1Marking>FH 1</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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				</Images>
			</Presentations>
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			<brandname>Hygroton</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>11035</Austr>
				<PresentationName>Hygroton 25</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
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							<DoseForm>Tablets</DoseForm>
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		</Brand><Brand>
			<brandname>Hyoscine Butylbromide (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>216124</Austr>
				<PresentationName>Pharmacy Action Stomach Ease Forte</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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		</Brand><Brand>
			<brandname>Hypnodorm</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>78344</Austr>
				<PresentationName>Hypnodorm</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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			</Presentations>
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			<brandname>Hysone</brandname>
			<isamtbrand>true</isamtbrand>
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				<Austr>27923</Austr>
				<PresentationName>Hysone</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Hydrocortisone</TGAIngredient>
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								<ImageFileName>27923-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>27926</Austr>
				<PresentationName>Hysone</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Hydrocortisone</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Scoring>scored</Scoring>
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			</Presentations>
		</Brand><Brand>
			<brandname>I-Pantoprazole</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>158200</Austr>
				<PresentationName>I-Pantoprazole</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Side2Marking></Side2Marking>
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							<View>
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			</Presentations>
			<Presentations>
				<Austr>158201</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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					<Versions>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158201-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ialex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>100143</Austr>
				<PresentationName>Ialex</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>GP1</Side1Marking>
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							<Views>
							<View>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>100144</Austr>
				<PresentationName>Ialex</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Cephalexin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateEffective>20/11/2008 13:23</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>dark green and light green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>GP2</Side1Marking>
							<Side2Marking>GP2</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>100144-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ibavyr</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>222627</Austr>
				<PresentationName>Ibavyr</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Ribavirin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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   				<WithdrawalDate></WithdrawalDate>
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							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>94527-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ikorel</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>56845</Austr>
				<PresentationName>Ikorel</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nicorandil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Ikorel</DocumentName>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>IK 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>56845-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>56846</Austr>
				<PresentationName>Ikorel</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nicorandil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Ikorel</DocumentName>
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						<ActiveIngredient>nicorandil</ActiveIngredient>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>IK 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>56846-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ikotab</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>218689</Austr>
				<PresentationName>Ikotab</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>nicorandil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Ikotab</DocumentName>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>nicorandil</ActiveIngredient>
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						<VersionSequence>1</VersionSequence>
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						<DateEffective>30/06/2021 14:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>218689-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>218690</Austr>
				<PresentationName>Ikotab</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>nicorandil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Ikotab</DocumentName>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/06/2021 14:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>218690-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Imatinib mesilate (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>261054</Austr>
				<PresentationName>Imatinib Apotex</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange to grayish-orange opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>RDY</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>261054-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>261060</Austr>
				<PresentationName>Imatinib Apotex</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/05/2017 13:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>very dark yellow to brownish-orange opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>RDY</Side1Marking>
							<Side2Marking>400</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>261060-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Imatinib mesilate (Teva)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>232234</Austr>
				<PresentationName>Imatinib-Teva</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>imatinib mesilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Imatinib-Teva</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>imatinib mesilate</ActiveIngredient>
						<ReleaseDate>2021-07-02 12:13:34.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/09/2022 11:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark yellow to brownish orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>IT 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>232234-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>232242</Austr>
				<PresentationName>Imatinib-Teva</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>imatinib mesilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Imatinib-Teva</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>imatinib mesilate</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/09/2022 11:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark yellow to brownish orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>IT 4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>232242-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Imdur</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>46390</Austr>
				<PresentationName>Imdur</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Isosorbide mononitrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Imdur</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ixcimdur10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>isosorbide mononitrate</ActiveIngredient>
						<ReleaseDate>2022-06-28 08:44:48.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 11:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>A ID</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>46390-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>62795</Austr>
				<PresentationName>Imdur</PresentationName>
    			<PresentionStrength>120mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Isosorbide mononitrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Imdur</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ixcimdur10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>isosorbide mononitrate</ActiveIngredient>
						<ReleaseDate>2022-06-28 08:44:48.0</ReleaseDate>
					</DocumentQualifiers>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 11:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>A IF</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62795-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Imigran</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>106714</Austr>
				<PresentationName>Imigran FDT</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sumatriptan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 15:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>triangular</Shape>
							<Side1Marking>GS 1YM</Side1Marking>
							<Side2Marking>50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>106714-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>106715</Austr>
				<PresentationName>Imigran FDT</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sumatriptan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 15:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>triangular</Shape>
							<Side1Marking>GS YE7</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>106715-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>38346</Austr>
				<PresentationName>Imigran Tablets</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sumatriptan succinate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>GX ET2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>38346-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>52261</Austr>
				<PresentationName>Imigran Tablets</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sumatriptan succinate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 15:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>GX ES3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>52261-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Imoclone</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>292090</Austr>
				<PresentationName>Imoclone</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/10/2018 16:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>292090-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Imovane</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>165934</Austr>
				<PresentationName>Imovane</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Zopiclone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Imovane</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>zopiclone</ActiveIngredient>
						<ReleaseDate>2022-02-07 10:26:18.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2010 14:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>165934-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Improvil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>62139</Austr>
				<PresentationName>Improvil 28 day</PresentationName>
    			<PresentionStrength>0.035mg/0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Norethisterone,Ethinyloestradiol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/09/2011 11:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>BX</Side1Marking>
							<Side2Marking>SEARLE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62139-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>BX</Side1Marking>
							<Side2Marking>SEARLE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62139-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>3</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>P</Side1Marking>
							<Side2Marking>SEARLE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62139-C03-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Imrest</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>99794</Austr>
				<PresentationName>Imrest</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Zopiclone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Imrest</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcimres20622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>zopiclone</ActiveIngredient>
						<ReleaseDate>2022-06-21 11:02:34.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>Z Z</Side1Marking>
							<Side2Marking>7.5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>99794-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Imtrate</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>59615</Austr>
				<PresentationName>Imtrate</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 12:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>cream</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>59615-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Imuran</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>31393</Austr>
				<PresentationName>Imuran Tablets</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Azathioprine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 13:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>GX EL5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>31393-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>31398</Austr>
				<PresentationName>Imuran Tablets</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Azathioprine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 13:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>GX CH1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>31398-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Indapamide (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167015</Austr>
				<PresentationName>Indapamide-GA</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 11:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167015-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Indapamide Hemihydrate (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>208007</Austr>
				<PresentationName>APO-Indapamide SR</PresentationName>
    			<PresentionStrength>1.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Indapamide hemihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>208007-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Indapamide Hemihydrate (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167028</Austr>
				<PresentationName>Chemmart Indapamide</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Indapamide hemihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/11/2010 11:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167028-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>75573</Austr>
				<PresentationName>Chemmart Indapamide</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Indapamide hemihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/08/2008 10:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>n</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75573-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Indapamide Hemihydrate (GenRx)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167027</Austr>
				<PresentationName>GenRx Indapamide</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Indapamide hemihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167027-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>75574</Austr>
				<PresentationName>GenRx Indapamide</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Indapamide hemihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/08/2008 09:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>n</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75574-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Indapamide Hemihydrate (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>169291</Austr>
				<PresentationName>Indapamide Sandoz</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
				<Austr>75571</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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				<Austr>76021</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<brandname>Inlyta</brandname>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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			<Presentations>
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			<Presentations>
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				<PresentationName>Insig</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184244-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Inspra</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>100162</Austr>
				<PresentationName>Inspra</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Eplerenone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Inspra</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocinspt11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>eplerenone</ActiveIngredient>
						<ReleaseDate>2021-10-22 11:55:56.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/09/2011 11:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>arc diamond</Shape>
							<Side1Marking>NSR 25</Side1Marking>
							<Side2Marking>Pfizer</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>100162-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>100163</Austr>
				<PresentationName>Inspra</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Eplerenone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Inspra</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocinspt11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>eplerenone</ActiveIngredient>
						<ReleaseDate>2021-10-22 11:55:56.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/08/2008 11:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>arc diamond</Shape>
							<Side1Marking>NSR 50</Side1Marking>
							<Side2Marking>Pfizer</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>100163-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Intelence</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>176557</Austr>
				<PresentationName>Intelence</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Intelence</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jccintel10917</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>etravirine</ActiveIngredient>
						<ReleaseDate>2017-09-08 13:27:19.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/02/2012 16:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>T200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>176557-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Intuniv</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>275278</Austr>
				<PresentationName>Intuniv</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>guanfacine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Intuniv</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tkcintun11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>guanfacine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-19 13:13:15.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/09/2019 09:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>503</Side1Marking>
							<Side2Marking>1MG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>275278-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>275313</Austr>
				<PresentationName>Intuniv</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>guanfacine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Intuniv</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tkcintun11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>guanfacine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-19 13:13:15.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/09/2019 09:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>503</Side1Marking>
							<Side2Marking>2MG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>275313-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>275314</Austr>
				<PresentationName>Intuniv</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>guanfacine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Intuniv</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tkcintun11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>guanfacine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-19 13:13:15.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/09/2019 09:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>503</Side1Marking>
							<Side2Marking>3MG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>275314-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>275315</Austr>
				<PresentationName>Intuniv</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>guanfacine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Intuniv</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tkcintun11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>guanfacine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-19 13:13:15.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/09/2019 09:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>503</Side1Marking>
							<Side2Marking>4MG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>275315-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Invega</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>130502</Austr>
				<PresentationName>Invega</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Invega</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jccinveg10820</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>paliperidone</ActiveIngredient>
						<ReleaseDate>2020-08-11 14:45:05.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/07/2008 08:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PAL 3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>130502-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>130714</Austr>
				<PresentationName>Invega</PresentationName>
    			<PresentionStrength>6mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Invega</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jccinveg10820</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>paliperidone</ActiveIngredient>
						<ReleaseDate>2020-08-11 14:45:05.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/07/2008 08:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PAL 6</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>130714-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>130717</Austr>
				<PresentationName>Invega</PresentationName>
    			<PresentionStrength>9mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Invega</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jccinveg10820</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>paliperidone</ActiveIngredient>
						<ReleaseDate>2020-08-11 14:45:05.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/07/2008 08:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PAL 9</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>130717-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Invirase</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>119419</Austr>
				<PresentationName>Invirase</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Saquinavir mesylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Invirase</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>rocinvir10119</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>saquinavir mesilate</ActiveIngredient>
						<ReleaseDate>2019-01-18 16:14:11.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 15:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light orange to brownish orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SQV 500</Side1Marking>
							<Side2Marking>ROCHE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>119419-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Inza</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>40927</Austr>
				<PresentationName>Inza</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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							<Side1Marking>L174</Side1Marking>
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							<Views>
							<View>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
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			<Presentations>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>259884-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>259885</Austr>
				<PresentationName>Blooms the Chemist Irbesartan</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/05/2017 11:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L174</Side1Marking>
							<Side2Marking>300</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>259885-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Irbesartan (Chemmart)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>169790</Austr>
				<PresentationName>Chemmart Irbesartan</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>IRB 300</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>169790-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>169791</Austr>
				<PresentationName>Chemmart Irbesartan</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>IRB 75</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>169791-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216056</Austr>
				<PresentationName>Chemmart Irbesartan</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L172</Side1Marking>
							<Side2Marking>75</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216056-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216057</Austr>
				<PresentationName>Chemmart Irbesartan</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L173</Side1Marking>
							<Side2Marking>150</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216057-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216058</Austr>
				<PresentationName>Chemmart Irbesartan</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L174</Side1Marking>
							<Side2Marking>300</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216058-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Irbesartan (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>192794</Austr>
				<PresentationName>Irbesartan-GA</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 11:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L173</Side1Marking>
							<Side2Marking>150</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192794-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>192800</Austr>
				<PresentationName>Irbesartan-GA</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 11:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L172</Side1Marking>
							<Side2Marking>75</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192800-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>192805</Austr>
				<PresentationName>Irbesartan-GA</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 11:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L174</Side1Marking>
							<Side2Marking>300</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192805-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Irbesartan (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>191084</Austr>
				<PresentationName>Irbesartan GH</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/04/2017 16:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>I3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>191084-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>191404</Austr>
				<PresentationName>Irbesartan GH</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/04/2017 16:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>I2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>191404-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>191408</Austr>
				<PresentationName>Irbesartan GH</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/04/2017 16:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>I1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>191408-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Irbesartan (Mylan)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>214577</Austr>
				<PresentationName>Irbesartan Mylan</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>IN1</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214577-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>214579</Austr>
				<PresentationName>Irbesartan Mylan</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>IN2</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214579-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>214581</Austr>
				<PresentationName>Irbesartan Mylan</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>IN3</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214581-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Irbesartan (Ranbaxy)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>190475</Austr>
				<PresentationName>Irbesartan RBX</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/09/2013 13:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>I3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>190475-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>190478</Austr>
				<PresentationName>Irbesartan RBX</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/09/2013 13:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>I4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>190478-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>190482</Austr>
				<PresentationName>Irbesartan RBX</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 15:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>I5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>190482-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Irbesartan (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167406</Austr>
				<PresentationName>Irbesartan Sandoz</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/08/2013 14:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>75</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167406-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>167407</Austr>
				<PresentationName>Irbesartan Sandoz</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/08/2013 14:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167407-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>167409</Austr>
				<PresentationName>Irbesartan Sandoz</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/08/2013 14:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167409-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Irbesartan (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>169788</Austr>
				<PresentationName>Terry White Chemists Irbesartan</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>IRB 75</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>169788-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>169794</Austr>
				<PresentationName>Terry White Chemists Irbesartan</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>IRB 300</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>169794-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216059</Austr>
				<PresentationName>Terry White Chemists Irbesartan</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L172</Side1Marking>
							<Side2Marking>75</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216059-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216060</Austr>
				<PresentationName>Terry White Chemists Irbesartan</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L173</Side1Marking>
							<Side2Marking>150</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216060-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216061</Austr>
				<PresentationName>Terry White Chemists Irbesartan</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L174</Side1Marking>
							<Side2Marking>300</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216061-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Irbesartan HCT (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>190115</Austr>
				<PresentationName>Irbesartan HCT GH</PresentationName>
    			<PresentionStrength>150mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/04/2017 16:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>IT1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>190115-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>190117</Austr>
				<PresentationName>Irbesartan HCT GH</PresentationName>
    			<PresentionStrength>300mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/04/2017 16:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>tan</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>IT3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>190117-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>190124</Austr>
				<PresentationName>Irbesartan HCT GH</PresentationName>
    			<PresentionStrength>300mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/04/2017 16:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>IT2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>190124-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Irbesartan HCTZ (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>192829</Austr>
				<PresentationName>Irbesartan HCTZ AN</PresentationName>
    			<PresentionStrength>300mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pinkish brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L185</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192829-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>192834</Austr>
				<PresentationName>Irbesartan HCTZ AN</PresentationName>
    			<PresentionStrength>300mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L184</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192834-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>192837</Austr>
				<PresentationName>Irbesartan HCTZ AN</PresentationName>
    			<PresentionStrength>150mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L183</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192837-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Irbesartan HCTZ (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>175200</Austr>
				<PresentationName>APO-Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>300mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-09-20 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>300/12.5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>175200-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>175202</Austr>
				<PresentationName>APO-Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>300mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-09-20 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>300/25</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>175202-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>175211</Austr>
				<PresentationName>APO-Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>150mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-09-20 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>150/12.5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>175211-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>213302</Austr>
				<PresentationName>APO-Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>150mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 10:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L183</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>213302-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>213303</Austr>
				<PresentationName>APO-Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>300mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 10:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L184</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>213303-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>213305</Austr>
				<PresentationName>APO-Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>300mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 10:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pinkish brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L185</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>213305-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Irbesartan HCTZ (Blooms the Chemist)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>259572</Austr>
				<PresentationName>Blooms the Chemist Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>150mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/05/2017 11:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L183</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>259572-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>259592</Austr>
				<PresentationName>Blooms the Chemist Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>300mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/05/2017 11:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L184</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>259592-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>259612</Austr>
				<PresentationName>Blooms the Chemist Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>300mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/05/2017 11:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pinkish brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L185</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>259612-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Irbesartan HCTZ (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>175201</Austr>
				<PresentationName>Chemmart Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>150mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>150/12.5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>175201-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>175204</Austr>
				<PresentationName>Chemmart Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>300mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>300/12.5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>175204-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>175207</Austr>
				<PresentationName>Chemmart Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>300mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>300/25</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>175207-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216080</Austr>
				<PresentationName>Chemmart Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>150mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L183</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216080-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216081</Austr>
				<PresentationName>Chemmart Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>300mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L184</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216081-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216082</Austr>
				<PresentationName>Chemmart Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>300mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pinkish brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L185</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216082-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Irbesartan HCTZ (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>192823</Austr>
				<PresentationName>Irbesartan HCTZ-GA</PresentationName>
    			<PresentionStrength>150mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 11:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L183</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192823-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>192835</Austr>
				<PresentationName>Irbesartan HCTZ-GA</PresentationName>
    			<PresentionStrength>300mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 11:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pinkish brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L185</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192835-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>192841</Austr>
				<PresentationName>Irbesartan HCTZ-GA</PresentationName>
    			<PresentionStrength>300mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 11:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L184</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192841-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Irbesartan HCTZ (Ranbaxy)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>190460</Austr>
				<PresentationName>Irbesartan HCTZ RBX</PresentationName>
    			<PresentionStrength>300mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>IH 3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>190460-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>190466</Austr>
				<PresentationName>Irbesartan HCTZ RBX</PresentationName>
    			<PresentionStrength>300/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink/red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>IH 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>190466-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>190470</Austr>
				<PresentationName>Irbesartan HCTZ RBX</PresentationName>
    			<PresentionStrength>150mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/09/2013 13:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink/red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>IH 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>190470-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Irbesartan HCTZ (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>175209</Austr>
				<PresentationName>Terry White Chemists Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>300mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>300/12.5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>175209-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>175212</Austr>
				<PresentationName>Terry White Chemists Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>300mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>300/25</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>175212-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>175213</Austr>
				<PresentationName>Terry White Chemists Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>150mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>150/12.5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>175213-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216083</Austr>
				<PresentationName>Terry White Chemists Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>150mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L183</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216083-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216084</Austr>
				<PresentationName>Terry White Chemists Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>300mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L184</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216084-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216085</Austr>
				<PresentationName>Terry White Chemists Irbesartan HCTZ</PresentationName>
    			<PresentionStrength>300mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pinkish brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L185</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216085-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Irbesartan/HCT (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>174724</Austr>
				<PresentationName>Irbesartan/HCT Sandoz</PresentationName>
    			<PresentionStrength>300mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/08/2013 14:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>apricot</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>300H</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>174724-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>174729</Austr>
				<PresentationName>Irbesartan/HCT Sandoz</PresentationName>
    			<PresentionStrength>150mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/08/2013 14:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>apricot</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>150H</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>174729-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>174731</Austr>
				<PresentationName>Irbesartan/HCT Sandoz</PresentationName>
    			<PresentionStrength>300mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/08/2013 14:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>25 H</Side1Marking>
							<Side2Marking>300</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>174731-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Iressa</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>90010</Austr>
				<PresentationName>Iressa</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gefitinib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Iressa</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apciress10121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>gefitinib</ActiveIngredient>
						<ReleaseDate>2021-01-21 09:02:16.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 11:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>IRESSA 250</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>90010-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Iscover</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>79021</Austr>
				<PresentationName>Iscover</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clopidogrel hydrogen sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Iscover</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swciscov10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clopidogrel </ActiveIngredient>
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				<Austr>12801</Austr>
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							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75240-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Isosorbide Mononitrate (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>75239</Austr>
				<PresentationName>Chemmart Isosorbide Mononitrate</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Isosorbide mononitrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/07/2008 11:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>cream</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75239-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Isosorbide Mononitrate (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>75237</Austr>
				<PresentationName>Terry White Chemists Isosorbide Mononitrate</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Isosorbide mononitrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/07/2008 11:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>cream</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75237-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Isotretinoin (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>186339</Austr>
				<PresentationName>Isotretinoin AN</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2017 16:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light violet</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>186339-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>186340</Austr>
				<PresentationName>Isotretinoin AN</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>26/07/2017 16:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>maroon</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>186340-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Isotretinoin (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>190940</Austr>
				<PresentationName>APO-Isotretinoin</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Isotretinoin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/09/2012 09:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red-orange</Colour>
							<Scoring></Scoring>
							<Shape>oval</Shape>
							<Side1Marking>P10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>190940-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>190941</Austr>
				<PresentationName>APO-Isotretinoin</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Isotretinoin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/09/2012 09:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red-orange</Colour>
							<Scoring></Scoring>
							<Shape>oval</Shape>
							<Side1Marking>P20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>190941-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Isotretinoin (SCP)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>165116</Austr>
				<PresentationName>Isotretinoin SCP</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/12/2013 15:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red-orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>P10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>165116-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>165123</Austr>
				<PresentationName>Isotretinoin SCP</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/12/2013 15:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red-orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>P20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>165123-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Itracap</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>244472</Austr>
				<PresentationName>Itracap</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Itraconazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Itracap</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcitrac11122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>itraconazole</ActiveIngredient>
						<ReleaseDate>2022-11-03 09:25:52.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/12/2018 16:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>ITR</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>244472-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Itraconazole (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>244473</Austr>
				<PresentationName>APO-Itraconazole</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>itraconazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/07/2017 15:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>ITR</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>244473-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Itranox</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>244432</Austr>
				<PresentationName>Itranox</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/04/2018 15:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>ITR</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>244432-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ivabradine hydrochloride (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>285493</Austr>
				<PresentationName>APO-Ivabradine</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>ivabradine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/11/2018 19:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light salmon</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>285493-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>285496</Austr>
				<PresentationName>APO-Ivabradine</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>ivabradine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/11/2018 19:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light salmon</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>285496-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Jadenu</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>286751</Austr>
				<PresentationName>Jadenu</PresentationName>
    			<PresentionStrength>90mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Deferasirox</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Jadenu</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
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						<ActiveIngredient>deferasirox</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/03/2019 10:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>ovaloid</Shape>
							<Side1Marking>90 between 2 curved lines</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>286761</Austr>
				<PresentationName>Jadenu</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Deferasirox</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Jadenu</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
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						<ActiveIngredient>deferasirox</ActiveIngredient>
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						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>medium blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>ovaloid</Shape>
							<Side1Marking>180 between 2 curved lines</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>293497</Austr>
				<PresentationName>Jadenu</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>ovaloid</Shape>
							<Side1Marking>360 between 2 curved lines</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Jakavi</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>198933</Austr>
				<PresentationName>Jakavi</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ruxolitinib phosphate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Jakavi</DocumentName>
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								<Format>PDF</Format>
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						<ActiveIngredient>ruxolitinib phosphate</ActiveIngredient>
						<ReleaseDate>2022-10-19 10:34:29.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>26/03/2014 13:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to almost white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elongated</Shape>
							<Side1Marking>L20</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>198933-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>198934</Austr>
				<PresentationName>Jakavi</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ruxolitinib phosphate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Jakavi</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcjakor11022</Filename>
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						<ActiveIngredient>ruxolitinib phosphate</ActiveIngredient>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/03/2014 13:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to almost white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L5</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>198934-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>198936</Austr>
				<PresentationName>Jakavi</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ruxolitinib phosphate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Jakavi</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcjakor11022</Filename>
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						</DocumentTypes>
						<ActiveIngredient>ruxolitinib phosphate</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>26/03/2014 13:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to almost white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>ovaloid</Shape>
							<Side1Marking>L15</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>198936-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>232702</Austr>
				<PresentationName>Jakavi</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ruxolitinib phosphate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Jakavi</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcjakor11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ruxolitinib phosphate</ActiveIngredient>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>22/05/2017 15:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to almost white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L10</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>232702-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Janumet</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>149014</Austr>
				<PresentationName>Janumet</PresentationName>
    			<PresentionStrength>50mg/500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sitagliptin phosphate monohydrate,Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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							<AvailableFormats>
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						<ActiveIngredient>sitagliptin phosphate monohydrate with metformin hydrochloride</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>575</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>149014-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>149021</Austr>
				<PresentationName>Janumet</PresentationName>
    			<PresentionStrength>50mg/850mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sitagliptin phosphate monohydrate,Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Janumet</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>sitagliptin phosphate monohydrate with metformin hydrochloride</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/03/2010 08:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>515</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>149021-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>149023</Austr>
				<PresentationName>Janumet</PresentationName>
    			<PresentionStrength>50mg/1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride,Sitagliptin phosphate monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Janumet</DocumentName>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>sitagliptin phosphate monohydrate with metformin hydrochloride</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/03/2010 08:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>577</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>149023-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>205317</Austr>
				<PresentationName>Janumet XR</PresentationName>
    			<PresentionStrength>50mg/1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Sitagliptin phosphate monohydrate,Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Janumet XR</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>sitagliptin phosphate monohydrate with metformin hydrochloride</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>11/08/2014 14:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>80</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>205317-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
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			</Presentations>
			<Presentations>
				<Austr>205318</Austr>
				<PresentationName>Janumet XR</PresentationName>
    			<PresentionStrength>100mg/1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Sitagliptin phosphate monohydrate,Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Janumet XR</DocumentName>
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							<AvailableFormats>
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					<Versions>
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						<DateEffective>11/08/2014 14:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>81</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>205318-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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			</Presentations>
		</Brand><Brand>
			<brandname>Januvia</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>133182</Austr>
				<PresentationName>Januvia</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sitagliptin phosphate monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Januvia</DocumentName>
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						<ActiveIngredient>Sitagliptin phosphate monohydrate</ActiveIngredient>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/10/2008 12:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
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							<Side1Marking>277</Side1Marking>
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							<View>
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			<Presentations>
				<Austr>133187</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>Sitagliptin phosphate monohydrate</ActiveIngredient>
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					<Versions>
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			<Presentations>
				<Austr>133188</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133188-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Jardiamet</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>229815</Austr>
				<PresentationName>Jardiamet</PresentationName>
    			<PresentionStrength>5mg/500mg</PresentionStrength>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>metformin hydrochloride,empagliflozin</TGAIngredient>
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				<Documents>
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							<PhaseItem>1</PhaseItem>
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							<Shape>oval</Shape>
							<Side1Marking>BI symbol S5</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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			<Presentations>
				<Austr>229817</Austr>
				<PresentationName>Jardiamet</PresentationName>
    			<PresentionStrength>5mg/1000mg</PresentionStrength>
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   				<WithdrawalDate></WithdrawalDate>
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							<PhaseItem>1</PhaseItem>
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							<Side1Marking>BI symbol S5</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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			<Presentations>
				<Austr>229818</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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							<PhaseItem>1</PhaseItem>
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			<Presentations>
				<Austr>229820</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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					<DocumentQualifiers>
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						<DocumentName>Jardiamet</DocumentName>
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							<PhaseItem>1</PhaseItem>
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			</Presentations>
		</Brand><Brand>
			<brandname>Jardiance</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>208827</Austr>
				<PresentationName>Jardiance</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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						<DocumentName>Jardiance</DocumentName>
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			<Presentations>
				<Austr>208829</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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					<Versions>
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		</Brand><Brand>
			<brandname>Jinarc</brandname>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>composite pack</Container>
    			<TGAIngredient>Tolvaptan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Jinarc</DocumentName>
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							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tolvaptan</ActiveIngredient>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/09/2019 19:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified rectangular</Shape>
							<Side1Marking>OTSUKA 60</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>272788-C01-01-BL600.jpg</ImageFileName>
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							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>OTSUKA 30</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>272788-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>272789</Austr>
				<PresentationName>Jinarc</PresentationName>
    			<PresentionStrength>30mg+90mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>composite pack</Container>
    			<TGAIngredient>Tolvaptan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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					</DocumentQualifiers>
				</Documents>
				<Images>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>pentagonal</Shape>
							<Side1Marking>OTSUKA 90</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>272789-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>OTSUKA 30</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>272789-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Joncia</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>176508</Austr>
				<PresentationName>Joncia</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>milnacipran hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Joncia </DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fbcjonci10220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>milnacipran hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-02-26 21:30:13.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/11/2020 16:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>PFM</Side1Marking>
							<Side2Marking>25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>176508-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>176513</Austr>
				<PresentationName>Joncia</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>milnacipran hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Joncia </DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fbcjonci10220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>milnacipran hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-02-26 21:30:13.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/11/2020 16:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>PFM</Side1Marking>
							<Side2Marking>50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>176513-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Juliet</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>75554</Austr>
				<PresentationName>Juliet-35ED</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2010 09:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75554-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75554-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Juluca</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>291356</Austr>
				<PresentationName>Juluca</PresentationName>
    			<PresentionStrength>50mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Dolutegravir,rilpivirine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Juluca</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>vicjuluc10721</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>dolutegravir with rilpivirine</ActiveIngredient>
						<ReleaseDate>2021-07-06 10:45:53.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2020 11:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SV J3T</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>291356-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Jurnista</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>141508</Austr>
				<PresentationName>Jurnista</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Jurnista</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jccjurni11020</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>hydromorphone hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-10-16 16:38:26.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/07/2010 13:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>HM 8</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>141508-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>141533</Austr>
				<PresentationName>Jurnista</PresentationName>
    			<PresentionStrength>16mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Jurnista</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jccjurni11020</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>hydromorphone hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-10-16 16:38:26.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>10/09/2009 16:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>HM 16</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>141533-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>141534</Austr>
				<PresentationName>Jurnista</PresentationName>
    			<PresentionStrength>32mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Jurnista</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jccjurni11020</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>hydromorphone hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-10-16 16:38:26.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>10/09/2009 16:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>HM 32</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>141534-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>141535</Austr>
				<PresentationName>Jurnista</PresentationName>
    			<PresentionStrength>64mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Jurnista</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jccjurni11020</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>hydromorphone hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-10-16 16:38:26.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>10/09/2009 16:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>HM 64</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>141535-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>155995</Austr>
				<PresentationName>Jurnista</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Jurnista</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jccjurni11020</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>hydromorphone hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-10-16 16:38:26.0</ReleaseDate>
					</DocumentQualifiers>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/11/2010 16:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>HM 4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>155995-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Juvicor</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>191478</Austr>
				<PresentationName>Juvicor</PresentationName>
    			<PresentionStrength>100mg/20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sitagliptin phosphate monohydrate,Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/08/2013 09:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink-beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified capsule shaped</Shape>
							<Side1Marking>MSD logo 757</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>191478-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>191481</Austr>
				<PresentationName>Juvicor</PresentationName>
    			<PresentionStrength>100mg/40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin,Sitagliptin phosphate monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/08/2013 09:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange-beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified capsule shaped</Shape>
							<Side1Marking>MSD logo 773</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>191481-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>191482</Austr>
				<PresentationName>Juvicor</PresentationName>
    			<PresentionStrength>100mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sitagliptin phosphate monohydrate,Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/08/2013 10:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink-beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>MSD logo 753</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>191482-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>K-Sol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>91558</Austr>
				<PresentationName>K-Sol</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>tube</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/01/2009 11:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white or white to yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>91558-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>91558-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Kaletra</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>121055</Austr>
				<PresentationName>Kaletra</PresentationName>
    			<PresentionStrength>200mg/50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Ritonavir,Lopinavir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kaletra</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>veckalet20820</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lopinavir with ritonavir</ActiveIngredient>
						<ReleaseDate>2020-08-24 14:38:41.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/11/2008 11:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>Abbott logo KA</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121055-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>140509</Austr>
				<PresentationName>Kaletra</PresentationName>
    			<PresentionStrength>100mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Ritonavir,Lopinavir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kaletra</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>veckalet20820</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lopinavir with ritonavir</ActiveIngredient>
						<ReleaseDate>2020-08-24 14:38:41.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/11/2008 11:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>Abbott logo KC</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>140509-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Kalixocin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>99707</Austr>
				<PresentationName>Kalixocin</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clarithromycin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kalixocin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gockalix10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clarithromycin</ActiveIngredient>
						<ReleaseDate>2022-05-12 15:22:19.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>99707-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Kalma</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>46835</Austr>
				<PresentationName>Kalma</PresentationName>
    			<PresentionStrength>0.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Alprazolam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kalma</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afckalma10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>alprazolam</ActiveIngredient>
						<ReleaseDate>2022-09-02 10:49:21.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>AL 0.25</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>46835-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>46837</Austr>
				<PresentationName>Kalma</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Alprazolam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kalma</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afckalma10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>alprazolam</ActiveIngredient>
						<ReleaseDate>2022-09-02 10:49:21.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>AL 0.5</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>46837-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>46839</Austr>
				<PresentationName>Kalma</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Alprazolam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kalma</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afckalma10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>alprazolam</ActiveIngredient>
						<ReleaseDate>2022-09-02 10:49:21.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>AL 1.0</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>46839-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>63993</Austr>
				<PresentationName>Kalma</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Alprazolam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kalma</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afckalma10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>alprazolam</ActiveIngredient>
						<ReleaseDate>2022-09-02 10:49:21.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/07/2022 15:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>A L</Side1Marking>
							<Side2Marking>G 2</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>63993-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Superceded</VersionStatus>
						<DateEffective>25/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>A L</Side1Marking>
							<Side2Marking>G 2</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>63993-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Kapanol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>48134</Austr>
				<PresentationName>Kapanol</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Morphine sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kapanol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ynckapan70221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>morphine sulfate pentahydrate</ActiveIngredient>
						<ReleaseDate>2021-02-17 13:54:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 15:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>clear with two black bands</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>K20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>48134-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>48135</Austr>
				<PresentationName>Kapanol</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Morphine sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kapanol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ynckapan70221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>morphine sulfate pentahydrate</ActiveIngredient>
						<ReleaseDate>2021-02-17 13:54:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 15:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>clear with three black bands</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>K50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>48135-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>48136</Austr>
				<PresentationName>Kapanol</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Morphine sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kapanol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ynckapan70221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>morphine sulfate pentahydrate</ActiveIngredient>
						<ReleaseDate>2021-02-17 13:54:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 15:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>clear with four black bands</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>K100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>48136-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>68439</Austr>
				<PresentationName>Kapanol</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Morphine sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kapanol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ynckapan70221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>morphine sulfate pentahydrate</ActiveIngredient>
						<ReleaseDate>2021-02-17 13:54:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 15:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>clear with one black band</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>K10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>68439-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Karlor</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>100160</Austr>
				<PresentationName>Karlor CD</PresentationName>
    			<PresentionStrength>375mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-06-15 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Cefaclor monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/12/2021 12:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>100160-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Superceded</VersionStatus>
						<DateEffective>20/11/2008 13:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>100160-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Karvea</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>101702</Austr>
				<PresentationName>Karvea</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Karvea</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swckarve10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>irbesartan</ActiveIngredient>
						<ReleaseDate>2022-08-30 17:29:06.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2013 11:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>2871</Side1Marking>
							<Side2Marking>heart shape</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101702-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101706</Austr>
				<PresentationName>Karvea</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Karvea</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swckarve10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>irbesartan</ActiveIngredient>
						<ReleaseDate>2022-08-30 17:29:06.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2013 11:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>2872</Side1Marking>
							<Side2Marking>heart shape</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101706-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101708</Austr>
				<PresentationName>Karvea</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Karvea</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swckarve10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>irbesartan</ActiveIngredient>
						<ReleaseDate>2022-08-30 17:29:06.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2013 11:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>2873</Side1Marking>
							<Side2Marking>heart shape</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101708-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Karvezide</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>101831</Austr>
				<PresentationName>Karvezide</PresentationName>
    			<PresentionStrength>150/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Irbesartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Karvezide</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swckarvz10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>irbesartan with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2022-09-07 09:31:24.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>2875</Side1Marking>
							<Side2Marking>heart shape</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101831-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101833</Austr>
				<PresentationName>Karvezide</PresentationName>
    			<PresentionStrength>300/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Karvezide</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swckarvz10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>irbesartan with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2022-09-07 09:31:24.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>2876</Side1Marking>
							<Side2Marking>heart shape</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101833-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>129442</Austr>
				<PresentationName>Karvezide</PresentationName>
    			<PresentionStrength>300/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Irbesartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Karvezide</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swckarvz10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>irbesartan with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2022-09-07 09:31:24.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>2788</Side1Marking>
							<Side2Marking>heart shape</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>129442-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Keflex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>73522</Austr>
				<PresentationName>Keflex (Aspen)</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Cephalexin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/11/2008 13:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>GP 1</Side1Marking>
							<Side2Marking>GP 1</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73522-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>73523</Austr>
				<PresentationName>Keflex (Aspen)</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Cephalexin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/11/2008 13:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>dark green and light green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>GP 2</Side1Marking>
							<Side2Marking>GP 2</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73523-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Keflor</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>58655</Austr>
				<PresentationName>Keflor CD</PresentationName>
    			<PresentionStrength>375mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Cefaclor monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Keflor CD</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afckefcd11020</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>cefaclor</ActiveIngredient>
						<ReleaseDate>2020-10-07 10:28:28.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>58655-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Keppra</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>120508</Austr>
				<PresentationName>Keppra</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/10/2008 12:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>ucb 250</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>120508-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>120509</Austr>
				<PresentationName>Keppra</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/10/2008 12:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>ucb 500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>120509-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>120513</Austr>
				<PresentationName>Keppra</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/10/2008 12:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>ucb 1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>120513-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Kevtam</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>278841</Austr>
				<PresentationName>Kevtam </PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Levetiracetam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kevtam (new formula)</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afckevtn11219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levetiracetam</ActiveIngredient>
						<ReleaseDate>2020-01-06 14:17:06.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/12/2018 10:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>278841-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>278842</Austr>
				<PresentationName>Kevtam </PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Levetiracetam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kevtam (new formula)</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afckevtn11219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levetiracetam</ActiveIngredient>
						<ReleaseDate>2020-01-06 14:17:06.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/12/2018 10:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>278842-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>278843</Austr>
				<PresentationName>Kevtam</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Levetiracetam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kevtam (new formula)</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afckevtn11219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levetiracetam</ActiveIngredient>
						<ReleaseDate>2020-01-06 14:17:06.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/12/2018 10:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>278843-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Kinson</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>49481</Austr>
				<PresentationName>Kinson</PresentationName>
    			<PresentionStrength>100mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Carbidopa,Levodopa</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kinson</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afckinso10922</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levodopa with carbidopa monohydrate</ActiveIngredient>
						<ReleaseDate>2022-09-15 12:51:03.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>LC 2</Side1Marking>
							<Side2Marking>&#945;</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>49481-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Kisqali</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>280246</Austr>
				<PresentationName>Kisqali</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>ribociclib succinate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kisqali</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvckisor10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ribociclib succinate</ActiveIngredient>
						<ReleaseDate>2022-06-09 12:35:30.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/02/2018 15:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light greyish violet</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RIC</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>280246-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Kivexa</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>99090</Austr>
				<PresentationName>Kivexa</PresentationName>
    			<PresentionStrength>600mg/300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Abacavir sulfate,Lamivudine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kivexa</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>vickivex10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>abacavir sulfate with lamivudine</ActiveIngredient>
						<ReleaseDate>2022-07-11 14:51:15.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 15:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>GS FC2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>99090-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Klacid</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>50682</Austr>
				<PresentationName>Klacid</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Clarithromycin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR>97190</IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/11/2008 09:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>50682-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>79564</Austr>
				<PresentationName>Klacid</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clarithromycin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Klacid</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocklaci10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clarithromycin</ActiveIngredient>
						<ReleaseDate>2022-05-12 15:22:24.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/11/2008 09:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>79564-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>79576</Austr>
				<PresentationName>Klacid</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Clarithromycin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/11/2008 10:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>79576-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Kliogest</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>183856</Austr>
				<PresentationName>Kliogest</PresentationName>
    			<PresentionStrength>2mg/1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>dial dispenser pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/09/2013 15:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NOVO 281</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183856-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>54472</Austr>
				<PresentationName>Kliogest</PresentationName>
    			<PresentionStrength>2mg/1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>dial dispenser pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/10/2008 09:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NOVO 281</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>54472-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Kliovance</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>67440</Austr>
				<PresentationName>Kliovance</PresentationName>
    			<PresentionStrength>1mg/0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>dial dispenser pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/10/2008 09:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NOVO 288</Side1Marking>
							<Side2Marking>Novo Nordisk logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>67440-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Kombiglyze</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>202207</Austr>
				<PresentationName>Kombiglyze XR</PresentationName>
    			<PresentionStrength>2.5mg/1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Saxagliptin,Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kombiglyze XR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apckomxr10219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>saxagliptin with metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2019-02-06 11:22:29.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/10/2014 10:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow to light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>4222</Side1Marking>
							<Side2Marking>2.5/1000</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>202207-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>202208</Austr>
				<PresentationName>Kombiglyze XR</PresentationName>
    			<PresentionStrength>5mg/1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride,Saxagliptin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kombiglyze XR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apckomxr10219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>saxagliptin with metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2019-02-06 11:22:29.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/10/2014 10:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>4223</Side1Marking>
							<Side2Marking>5/1000</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>202208-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>202209</Austr>
				<PresentationName>Kombiglyze XR</PresentationName>
    			<PresentionStrength>5mg/500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride,Saxagliptin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kombiglyze XR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apckomxr10219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>saxagliptin with metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2019-02-06 11:22:29.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/10/2014 10:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light brown to brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>4221</Side1Marking>
							<Side2Marking>5/500</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>202209-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Kosteo</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>234863</Austr>
				<PresentationName>Kosteo</PresentationName>
    			<PresentionStrength>0.25mcg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/05/2018 08:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red</Colour>
							<Scoring></Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234863-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Kudeq</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>211498</Austr>
				<PresentationName>Kudeq</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Celecoxib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/03/2015 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white with two blue bands</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>7767</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>211498-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>211499</Austr>
				<PresentationName>Kudeq</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Celecoxib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/03/2015 11:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white with two gold bands</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>7767</Side1Marking>
							<Side2Marking>200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>211499-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Kuvan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>165738</Austr>
				<PresentationName>Kuvan</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Sapropterin dihydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/03/2011 12:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white to light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>177</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>165738-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Kwells</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>82362</Austr>
				<PresentationName>Kwells</PresentationName>
    			<PresentionStrength>0.3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2009 14:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>apricot</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82362-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Kytril</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>60872</Austr>
				<PresentationName>Kytril Tablets</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Granisetron hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Kytril Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>iyckytrt10917</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>granisetron</ActiveIngredient>
						<ReleaseDate>2017-10-19 12:44:50.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 16:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>triangular</Shape>
							<Side1Marking>K2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>60872-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lacosam</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>296755</Austr>
				<PresentationName>Lacosam</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lacosam</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afclacos10322</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lacosamide</ActiveIngredient>
						<ReleaseDate>2022-03-29 11:09:52.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/11/2022 16:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>salmon</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L</Side1Marking>
							<Side2Marking>150</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>296755-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>296757</Austr>
				<PresentationName>Lacosam</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lacosam</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afclacos10322</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lacosamide</ActiveIngredient>
						<ReleaseDate>2022-03-29 11:09:52.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/11/2022 16:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>296757-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>296763</Austr>
				<PresentationName>Lacosam</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lacosam</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afclacos10322</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lacosamide</ActiveIngredient>
						<ReleaseDate>2022-03-29 11:09:52.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/11/2022 16:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L</Side1Marking>
							<Side2Marking>200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>296763-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>296765</Austr>
				<PresentationName>Lacosam</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lacosam</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afclacos10322</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lacosamide</ActiveIngredient>
						<ReleaseDate>2022-03-29 11:09:52.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/11/2022 16:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L</Side1Marking>
							<Side2Marking>50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>296765-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lamictal</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>51548</Austr>
				<PresentationName>Lamictal</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lamotrigine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/06/2011 09:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rounded square</Shape>
							<Side1Marking>GSCL5</Side1Marking>
							<Side2Marking>25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>51548-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>51549</Austr>
				<PresentationName>Lamictal</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lamotrigine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/06/2011 09:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rounded square</Shape>
							<Side1Marking>GSCL7</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>51549-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>51718</Austr>
				<PresentationName>Lamictal</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Lamotrigine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 15:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>long</Shape>
							<Side1Marking>GS CL2</Side1Marking>
							<Side2Marking>5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>51718-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>57190</Austr>
				<PresentationName>Lamictal</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lamotrigine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/06/2011 09:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rounded square</Shape>
							<Side1Marking>GSCX7</Side1Marking>
							<Side2Marking>50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>57190-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>57262</Austr>
				<PresentationName>Lamictal</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lamotrigine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/06/2011 09:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rounded square</Shape>
							<Side1Marking>GSEC5</Side1Marking>
							<Side2Marking>200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>57262-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>77098</Austr>
				<PresentationName>Lamictal</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Lamotrigine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/11/2008 09:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>LTG 2</Side1Marking>
							<Side2Marking>overlapping super-ellipses</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>77098-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lamidus</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>116720</Austr>
				<PresentationName>Lamidus</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/02/2009 11:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>LI 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>116720-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>116730</Austr>
				<PresentationName>Lamidus</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/02/2009 11:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>LI 3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>116730-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>116731</Austr>
				<PresentationName>Lamidus</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/02/2009 11:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>LI 4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>116731-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>116732</Austr>
				<PresentationName>Lamidus</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/02/2009 11:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>LI 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>116732-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>116732-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lamisil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>43523</Austr>
				<PresentationName>Lamisil Tablets</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Terbinafine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lamisil Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvclamor10220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>terbinafine hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-02-13 15:40:07.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/06/2011 09:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to yellow-tinged</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>LAMISIL 250</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>43523-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lamitan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>147631</Austr>
				<PresentationName>Lamitan</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified square-shaped</Shape>
							<Side1Marking>L 25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>147631-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>147632</Austr>
				<PresentationName>Lamitan</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified square-shaped</Shape>
							<Side1Marking>L 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>147632-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>147633</Austr>
				<PresentationName>Lamitan</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified square-shaped</Shape>
							<Side1Marking>L 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>147633-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>147634</Austr>
				<PresentationName>Lamitan</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified square-shaped</Shape>
							<Side1Marking>L 200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>147634-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lamivudine (Alphapharm)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167591</Austr>
				<PresentationName>Lamivudine Alphapharm</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Lamivudine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lamivudine Alphapharm</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afclamiv10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lamivudine</ActiveIngredient>
						<ReleaseDate>2022-02-16 13:59:04.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>M105</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167591-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>167594</Austr>
				<PresentationName>Lamivudine Alphapharm</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Lamivudine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lamivudine Alphapharm</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afclamiv10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lamivudine</ActiveIngredient>
						<ReleaseDate>2022-02-16 13:59:04.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>M300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167594-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lamivudine (Ranbaxy)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>172813</Austr>
				<PresentationName>Lamivudine RBX</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>modified diamond-shaped</Shape>
							<Side1Marking>RF 96</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>172813-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>172817</Austr>
				<PresentationName>Lamivudine RBX</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>grey</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified diamond-shaped</Shape>
							<Side1Marking>RF 97</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>172817-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lamivudine/Zidovudine (Viatris)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167477</Austr>
				<PresentationName>Lamivudine/Zidovudine Viatris 150/300</PresentationName>
    			<PresentionStrength>150mg/300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Zidovudine,Lamivudine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lamivudine/Zidovudine Viatris 150/300</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afclamzi11122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lamivudine with zidovudine</ActiveIngredient>
						<ReleaseDate>2022-11-10 17:10:24.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>M 103</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167477-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lamotrigine (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167520</Austr>
				<PresentationName>APO-Lamotrigine</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Lamotrigine,Calcium carbonate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/03/2011 13:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>LI 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167520-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>167521</Austr>
				<PresentationName>APO-Lamotrigine</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Lamotrigine,Calcium carbonate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/03/2011 13:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>LI 3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167521-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>167523</Austr>
				<PresentationName>APO-Lamotrigine</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lamotrigine,Calcium carbonate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/05/2012 11:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>LI 4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167523-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>167524</Austr>
				<PresentationName>APO-Lamotrigine</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Lamotrigine,Calcium carbonate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/03/2011 13:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>LI 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>167524-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>167524-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lamotrigine (AS)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>101354</Austr>
				<PresentationName>Lamotrigine-AS</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/12/2009 13:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified square shape</Shape>
							<Side1Marking>L 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101354-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101358</Austr>
				<PresentationName>Lamotrigine-AS</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/12/2009 13:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified square shape</Shape>
							<Side1Marking>L 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101358-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101368</Austr>
				<PresentationName>Lamotrigine-AS</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/12/2009 13:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified square shape</Shape>
							<Side1Marking>L 200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101368-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lamotrigine (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>143571</Austr>
				<PresentationName>Lamotrigine-GA</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 12:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified square shape</Shape>
							<Side1Marking>L 25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>143571-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>143572</Austr>
				<PresentationName>Lamotrigine-GA</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 14:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified square-shaped</Shape>
							<Side1Marking>L 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>143572-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>143573</Austr>
				<PresentationName>Lamotrigine-GA</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 14:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified square-shaped</Shape>
							<Side1Marking>L 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>143573-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>143585</Austr>
				<PresentationName>Lamotrigine-GA</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 14:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified square-shaped</Shape>
							<Side1Marking>L 200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>143585-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lamotrigine (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>129735</Austr>
				<PresentationName>Lamotrigine generichealth</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/11/2008 17:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>129735-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>129758</Austr>
				<PresentationName>Lamotrigine generichealth</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/11/2008 17:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>129758-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>129761</Austr>
				<PresentationName>Lamotrigine generichealth</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/09/2011 15:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>129761-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>129762</Austr>
				<PresentationName>Lamotrigine generichealth</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/11/2008 17:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>129762-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>129762-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lamotrigine (GenRx)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>101351</Austr>
				<PresentationName>GenRx Lamotrigine</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lamotrigine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/08/2008 09:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>square</Shape>
							<Side1Marking>L 25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101351-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101355</Austr>
				<PresentationName>GenRx Lamotrigine</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lamotrigine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/08/2008 09:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>square</Shape>
							<Side1Marking>L 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101355-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101365</Austr>
				<PresentationName>GenRx Lamotrigine</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lamotrigine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/08/2008 09:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>square</Shape>
							<Side1Marking>L 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101365-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101369</Austr>
				<PresentationName>GenRx Lamotrigine</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lamotrigine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/08/2008 09:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>square</Shape>
							<Side1Marking>L 200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101369-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lamotrigine (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>187254</Austr>
				<PresentationName>Lamotrigine Sandoz</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lamotrigine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rounded square-shaped</Shape>
							<Side1Marking>H</Side1Marking>
							<Side2Marking>77</Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>187254-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>187254-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>187261</Austr>
				<PresentationName>Lamotrigine Sandoz</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lamotrigine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rounded square-shaped</Shape>
							<Side1Marking>H</Side1Marking>
							<Side2Marking>80</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>187261-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>187272</Austr>
				<PresentationName>Lamotrigine Sandoz</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lamotrigine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rounded square-shaped</Shape>
							<Side1Marking>H</Side1Marking>
							<Side2Marking>79</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>187272-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>187278</Austr>
				<PresentationName>Lamotrigine Sandoz</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lamotrigine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 14:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rounded square-shaped</Shape>
							<Side1Marking>H</Side1Marking>
							<Side2Marking>78</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>187278-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>291469</Austr>
				<PresentationName>Sandoz Lamotrigine</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/08/2018 15:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>291469-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>291470</Austr>
				<PresentationName>Sandoz Lamotrigine</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>291470-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>291472</Austr>
				<PresentationName>Sandoz Lamotrigine</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<DateEffective>24/09/2018 16:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>291472-C01-01-BL600.jpg</ImageFileName>
							</View>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lamotrust</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>150747</Austr>
				<PresentationName>Lamotrust</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/12/2013 15:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>150747-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>150748</Austr>
				<PresentationName>Lamotrust</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/11/2013 15:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>150748-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>150749</Austr>
				<PresentationName>Lamotrust</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/02/2010 12:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>150749-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>150750</Austr>
				<PresentationName>Lamotrust</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/02/2010 12:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>150750-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>150750-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lanoxin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>11108</Austr>
				<PresentationName>Lanoxin PG</PresentationName>
    			<PresentionStrength>0.0625mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>U3A</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>11108-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>15333</Austr>
				<PresentationName>Lanoxin</PresentationName>
    			<PresentionStrength>0.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>X3A</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>15333-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lansoprazole (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>159345</Austr>
				<PresentationName>APO-Lansoprazole</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Lansoprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/11/2010 11:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>purple and lavender</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>L 30</Side1Marking>
							<Side2Marking>L 30</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159345-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216788</Austr>
				<PresentationName>APO-Lansoprazole ODT</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to yellowish white with orange speckles</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>I5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216788-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216794</Austr>
				<PresentationName>APO-Lansoprazole ODT</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to yellowish white with orange speckles</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>30</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>216794-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>216794-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lansoprazole (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>216792</Austr>
				<PresentationName>Lansoprazole ODT GH</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/04/2017 16:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to yellowish white, orange speckled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>30</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>216792-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>216792-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216793</Austr>
				<PresentationName>Lansoprazole ODT GH</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/04/2017 16:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to yellowish white, orange speckled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>15</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216793-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lanvis</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>11110</Austr>
				<PresentationName>Lanvis</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Thioguanine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/10/2010 08:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>cream</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>WELLCOME U3B</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>11110-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lanzopran</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>159343</Austr>
				<PresentationName>Lanzopran</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/06/2010 10:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>purple and lavender</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>L 30</Side1Marking>
							<Side2Marking>L 30</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159343-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Largactil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>51618</Austr>
				<PresentationName>Largactil</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Chlorpromazine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Largactil</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>chlorpromazine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-09-13 08:18:40.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/10/2008 11:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>LG 25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>51618-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>51619</Austr>
				<PresentationName>Largactil</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Chlorpromazine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Largactil</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swclarga10922</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>chlorpromazine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-09-13 08:18:40.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>LG 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>51619-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>51620</Austr>
				<PresentationName>Largactil</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Chlorpromazine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Largactil</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swclarga10922</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>chlorpromazine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-09-13 08:18:40.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>LG 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>51620-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lasix</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>12406</Austr>
				<PresentationName>Lasix</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Frusemide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lasix and Lasix High Dose</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swclasix10122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>furosemide (frusemide)</ActiveIngredient>
						<ReleaseDate>2022-02-09 15:30:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/09/2013 14:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Lasix 40</Side1Marking>
							<Side2Marking>HOECHST logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>12406-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>12409</Austr>
				<PresentationName>Lasix-M</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Frusemide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lasix and Lasix High Dose</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swclasix10122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>furosemide (frusemide)</ActiveIngredient>
						<ReleaseDate>2022-02-09 15:30:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/05/2021 08:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DLF</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>12409-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Latuda</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>206650</Austr>
				<PresentationName>Latuda</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>lurasidone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Latuda</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>seclatud10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lurasidone hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-07-18 09:46:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/10/2016 11:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L 40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>206650-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>206651</Austr>
				<PresentationName>Latuda</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>lurasidone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Latuda</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>seclatud10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lurasidone hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-07-18 09:46:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/10/2016 11:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L 80</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>206651-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lax-Tab</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>119101</Austr>
				<PresentationName>Lax-tab</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/09/2010 11:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>119101-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>119125</Austr>
				<PresentationName>Lax-tab</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/09/2010 14:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>119125-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Laxative with Senna (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>200805</Austr>
				<PresentationName>Pharmacy Action Laxative with Senna</PresentationName>
    			<PresentionStrength>50mg/8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>200805-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lecteva</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>238860</Austr>
				<PresentationName>Lecteva</PresentationName>
    			<PresentionStrength>50/12.5/ 200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Levodopa,carbidopa monohydrate,Entacapone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lecteva</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbclecte11020</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levodopa with carbidopa monohydrate and entacapone</ActiveIngredient>
						<ReleaseDate>2020-10-15 12:27:38.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>238860-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>238860-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>238861</Austr>
				<PresentationName>Lecteva</PresentationName>
    			<PresentionStrength>75/18.75/200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Entacapone,carbidopa monohydrate,Levodopa</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lecteva</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbclecte11020</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levodopa with carbidopa monohydrate and entacapone</ActiveIngredient>
						<ReleaseDate>2020-10-15 12:27:38.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>75</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>238861-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>238862</Austr>
				<PresentationName>Lecteva</PresentationName>
    			<PresentionStrength>100/25/200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Levodopa,Entacapone,carbidopa monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lecteva</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbclecte11020</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levodopa with carbidopa monohydrate and entacapone</ActiveIngredient>
						<ReleaseDate>2020-10-15 12:27:38.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>238862-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>238863</Austr>
				<PresentationName>Lecteva</PresentationName>
    			<PresentionStrength>125/31.25/200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>carbidopa monohydrate,Levodopa,Entacapone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lecteva</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbclecte11020</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levodopa with carbidopa monohydrate and entacapone</ActiveIngredient>
						<ReleaseDate>2020-10-15 12:27:38.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellowish brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>125</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>238863-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>238863-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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    			<PresentationForm>Tablets</PresentationForm>
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			<brandname>Leflunomide (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>210923</Austr>
				<PresentationName>Leflunomide AN</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient></TGAIngredient>
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							<Side2Marking></Side2Marking>
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			<Presentations>
				<Austr>210924</Austr>
				<PresentationName>Leflunomide AN</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
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			<brandname>Leflunomide (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>129482</Austr>
				<PresentationName>APO-Leflunomide</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-09-20 00:00:00'}</WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Leflunomide</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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							<Shape>round</Shape>
							<Side1Marking>LE 10</Side1Marking>
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							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>129538</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
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							<Side1Marking>LE 20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
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			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>471</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>219146-C02-01-BL600.jpg</ImageFileName>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lenest 30 ED</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>233113</Austr>
				<PresentationName>Lenest 30 ED</PresentationName>
    			<PresentionStrength>150mcg/30mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>composite pack</Container>
    			<TGAIngredient>Ethinyloestradiol,Levonorgestrel</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lenest 30 ED</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>levonorgestrel with ethinylestradiol</ActiveIngredient>
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						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/12/2018 10:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>711</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>233113-C01-01-BL600.jpg</ImageFileName>
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							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>274</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>233113-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lengout</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>97499</Austr>
				<PresentationName>Lengout</PresentationName>
    			<PresentionStrength>500mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Colchicine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/11/2008 13:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>97499-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lercadip</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>152709</Austr>
				<PresentationName>Lercadip</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-01-13 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lercanidipine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/04/2012 11:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152709-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>152710</Austr>
				<PresentationName>Lercadip</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-01-13 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lercanidipine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/04/2012 11:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152710-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lercan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>152707</Austr>
				<PresentationName>Lercan</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lercanidipine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/06/2011 13:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152707-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>152708</Austr>
				<PresentationName>Lercan</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lercanidipine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/06/2011 13:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152708-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lercanidipine (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>172204</Austr>
				<PresentationName>Lercanidipine Apotex</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>lercanidipine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 15:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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								<ViewLabel>C</ViewLabel>
								<ImageFileName>172204-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>172206</Austr>
				<PresentationName>Lercanidipine Apotex</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>lercanidipine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/10/2019 08:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>172206-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Lercanidipine (Blooms the Chemist)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>163766</Austr>
				<PresentationName>Blooms The Chemist Lercanidipine</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lercanidipine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 21:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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								<ImageFileName>163766-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
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			<Presentations>
				<Austr>163767</Austr>
				<PresentationName>Blooms The Chemist Lercanidipine</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lercanidipine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>22/05/2016 21:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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			</Presentations>
			<Presentations>
				<Austr>172209</Austr>
				<PresentationName>BTC Lercanidipine </PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>lercanidipine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/04/2020 09:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L</Side1Marking>
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							<Views>
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			</Presentations>
			<Presentations>
				<Austr>172210</Austr>
				<PresentationName>BTC Lercanidipine </PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>lercanidipine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/04/2020 09:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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								<ImageFileName>172210-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Lercanidipine (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>194780</Austr>
				<PresentationName>Lercanidipine GH</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>01/10/2013 11:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L</Side1Marking>
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							<Views>
							<View>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>194781</Austr>
				<PresentationName>Lercanidipine GH</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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								<ImageFileName>194781-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lescol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>82743</Austr>
				<PresentationName>Lescol XL</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluvastatin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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						<QualiferData></QualiferData>
						<DocumentName>Lescol XL</DocumentName>
						<DocumentTypes>
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						</DocumentTypes>
						<ActiveIngredient>fluvastatin sodium</ActiveIngredient>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>03/12/2008 11:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>LE</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82743-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Letrozole (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>159227</Austr>
				<PresentationName>Letrozole AN</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/12/2017 13:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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								<ImageFileName>159227-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Letrozole (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>163826</Austr>
				<PresentationName>APO-Letrozole</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-09-20 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Letrozole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 13:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>LET 2.5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>163826-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>309249</Austr>
				<PresentationName>Letrozole Apotex</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/03/2020 20:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>LT</Side1Marking>
							<Side2Marking>2.5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>309249-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Letrozole (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>174638</Austr>
				<PresentationName>Letrozole-GA</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/06/2012 08:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow to dark yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>174638-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Letrozole (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>176278</Austr>
				<PresentationName>Letrozole generichealth</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>176278-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Letrozole (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>159589</Austr>
				<PresentationName>Pharmacor Letrozole</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/10/2012 09:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159589-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Letrozole (Ranbaxy)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167832</Austr>
				<PresentationName>Letrozole RBX</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>LET1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167832-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Letrozole (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>172124</Austr>
				<PresentationName>Letrozole Sandoz</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Letrozole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Letrozole Sandoz</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcletor10520</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>letrozole</ActiveIngredient>
						<ReleaseDate>2020-06-10 14:35:33.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/04/2012 16:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CG</Side1Marking>
							<Side2Marking>FV</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>172124-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Letrozole (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>163827</Austr>
				<PresentationName>Terry White Chemists Letrozole</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Letrozole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
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						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 14:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>LET 2.5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>163827-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Leucovorin Calcium (DBL)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>16364</Austr>
				<PresentationName>DBL Leucovorin Calcium</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>calcium folinate hydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 16:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellowish-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C F</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>16364-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Leukeran</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>73026</Austr>
				<PresentationName>Leukeran</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Chlorambucil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/10/2010 08:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L</Side1Marking>
							<Side2Marking>GX EG3</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73026-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Levetiracetam (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>189879</Austr>
				<PresentationName>Levetiracetam AN</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/12/2017 13:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L 64</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>189879-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>189880</Austr>
				<PresentationName>Levetiracetam AN</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/12/2017 13:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L 65</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>189880-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>189881</Austr>
				<PresentationName>Levetiracetam AN</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L 67</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>189881-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Levetiracetam (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>156311</Austr>
				<PresentationName>APO-Levetiracetam</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-09-20 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Levetiracetam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/10/2010 09:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LEV 250</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156311-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156313</Austr>
				<PresentationName>APO-Levetiracetam</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-09-20 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Levetiracetam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/10/2010 09:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LEV 500</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156313-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156328</Austr>
				<PresentationName>APO-Levetiracetam</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-09-20 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Levetiracetam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/10/2010 09:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LEV 1000</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156328-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>296940</Austr>
				<PresentationName>APO-Levetiracetam</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>levetiracetam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/03/2020 22:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>296940-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>296941</Austr>
				<PresentationName>APO-Levetiracetam</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>levetiracetam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/03/2020 22:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>296941-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>296942</Austr>
				<PresentationName>APO-Levetiracetam</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>levetiracetam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/03/2020 22:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>296942-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Levetiracetam (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>156312</Austr>
				<PresentationName>Chemmart Levetiracetam</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Levetiracetam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/10/2010 11:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LEV 1000</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156312-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156316</Austr>
				<PresentationName>Chemmart Levetiracetam</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Levetiracetam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/10/2010 11:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LEV 500</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156316-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156318</Austr>
				<PresentationName>Chemmart Levetiracetam</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Levetiracetam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/10/2010 11:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LEV 250</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156318-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Levetiracetam (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>159047</Austr>
				<PresentationName>Levetiracetam generichealth</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/04/2015 16:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>1014</Side1Marking>
							<Side2Marking>250 MG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159047-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>159048</Austr>
				<PresentationName>Levetiracetam generichealth</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/04/2015 16:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>1015</Side1Marking>
							<Side2Marking>500 MG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159048-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>159049</Austr>
				<PresentationName>Levetiracetam generichealth</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/04/2015 16:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>1017</Side1Marking>
							<Side2Marking>1000 MG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159049-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>161295</Austr>
				<PresentationName>Levetiracetam-GH</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/04/2017 16:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>161295-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>161296</Austr>
				<PresentationName>Levetiracetam-GH</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/04/2017 16:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>161296-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Levetiracetam (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>159268</Austr>
				<PresentationName>Levetiracetam SZ</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/04/2012 16:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>LEV 250</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159268-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>159269</Austr>
				<PresentationName>Levetiracetam SZ</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/04/2012 16:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>LEV 500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159269-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>159271</Austr>
				<PresentationName>Levetiracetam SZ</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/04/2012 17:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>LEV 1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159271-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Levetiracetam (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>156310</Austr>
				<PresentationName>Terry White Chemists Levetiracetam</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Levetiracetam</TGAIngredient>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LEV 1000</Side1Marking>
							<Side2Marking>APO</Side2Marking>
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								<ViewLabel>C</ViewLabel>
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				<Austr>156319</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Levetiracetam</TGAIngredient>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LEV 500</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156319-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>156326</Austr>
				<PresentationName>Terry White Chemists Levetiracetam</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LEV 250</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156326-C01-01-BL600.jpg</ImageFileName>
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			<brandname>Levi</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>168790</Austr>
				<PresentationName>Levi</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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						<DateEffective>25/05/2018 08:49</DateEffective>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L 64</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>168790-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>168792</Austr>
				<PresentationName>Levi</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L 65</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>168792-C01-01-BL600.jpg</ImageFileName>
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			<Presentations>
				<Austr>168794</Austr>
				<PresentationName>Levi</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L 67</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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								<ImageFileName>168794-C01-01-BL600.jpg</ImageFileName>
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		</Brand><Brand>
			<brandname>Levitaccord</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>168789</Austr>
				<PresentationName>Levitaccord</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L 64</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>168793</Austr>
				<PresentationName>Levitaccord</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L 65</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>168793-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Levitra</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>90498</Austr>
				<PresentationName>Levitra</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>22/04/2010 11:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking>Bayer Cross</Side2Marking>
							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>90499</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking>Bayer Cross</Side2Marking>
							<Views>
							<View>
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			<Presentations>
				<Austr>90500</Austr>
				<PresentationName>Levitra</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Side1Marking>20</Side1Marking>
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							<Views>
							<View>
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			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>40193</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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				<Austr>149270</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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							<Views>
							<View>
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				<Austr>231121</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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							<Shape>round</Shape>
							<Side1Marking>LE4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>205575-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>205575-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lexam</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>211387</Austr>
				<PresentationName>Lexam</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>E 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>211387-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>211388</Austr>
				<PresentationName>Lexam</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>E 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>211388-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lexapro</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>92051</Austr>
				<PresentationName>Lexapro</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Escitalopram oxalate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lexapro Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>luclexat10322</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>escitalopram oxalate</ActiveIngredient>
						<ReleaseDate>2022-03-24 12:41:33.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/09/2008 11:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>E L</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>92051-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>92053</Austr>
				<PresentationName>Lexapro</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Escitalopram oxalate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lexapro Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>luclexat10322</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>escitalopram oxalate</ActiveIngredient>
						<ReleaseDate>2022-03-24 12:41:33.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/09/2008 11:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>E N</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>92053-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lexotan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>52269</Austr>
				<PresentationName>Lexotan</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bromazepam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/12/2010 11:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale red, slightly speckled</Colour>
							<Scoring>scored</Scoring>
							<Shape>cylindrical</Shape>
							<Side1Marking>ROCHE 3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>52269-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>52270</Austr>
				<PresentationName>Lexotan</PresentationName>
    			<PresentionStrength>6mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bromazepam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/09/2008 16:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>greenish-grey slightly speckled</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROCHE 6</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>52270-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lezole</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>184746</Austr>
				<PresentationName>Lezole</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 14:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>2.5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184746-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Linevox</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>237304</Austr>
				<PresentationName>Linevox</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/04/2018 15:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>600</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>237304-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lioresal</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>11038</Austr>
				<PresentationName>Lioresal Tablets</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Baclofen</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lioresal Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>baclofen</ActiveIngredient>
						<ReleaseDate>2022-03-18 16:56:41.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2010 12:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>KJ</Side1Marking>
							<Side2Marking>CG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>11038-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>11039</Austr>
				<PresentationName>Lioresal Tablets</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Baclofen</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2010 12:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>UR</Side1Marking>
							<Side2Marking>CG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>11039-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>68365</Austr>
				<PresentationName>Lioresal Tablets</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Baclofen</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lioresal Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>baclofen</ActiveIngredient>
						<ReleaseDate>2022-03-18 16:56:41.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2010 12:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>UR</Side1Marking>
							<Side2Marking>CG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>68365-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lipazil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>62742</Austr>
				<PresentationName>Lipazil</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 12:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>dp 600</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62742-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lipex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>11616</Austr>
				<PresentationName>Lipex</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lipex</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqclipex10221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>simvastatin</ActiveIngredient>
						<ReleaseDate>2021-04-19 15:07:05.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/11/2008 07:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MSD 735</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>11616-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>11617</Austr>
				<PresentationName>Lipex</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lipex</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						</DocumentTypes>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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			<Presentations>
				<Austr>59273</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<DocumentQualifiers>
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						<DocumentName>Lipex</DocumentName>
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							<PhaseItem>1</PhaseItem>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>65524</Austr>
				<PresentationName>Lipex</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lipex</DocumentName>
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						</DocumentTypes>
						<ActiveIngredient>simvastatin</ActiveIngredient>
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						<VersionSequence>1</VersionSequence>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brick-red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>543</Side1Marking>
							<Side2Marking>80</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>65524-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lipidil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>118634</Austr>
				<PresentationName>Lipidil</PresentationName>
    			<PresentionStrength>145mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fenofibrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lipidil</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fenofibrate</ActiveIngredient>
						<ReleaseDate>2021-12-03 08:08:19.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/09/2008 15:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>145</Side1Marking>
							<Side2Marking>Fournier logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>118634-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>118642</Austr>
				<PresentationName>Lipidil</PresentationName>
    			<PresentionStrength>48mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fenofibrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lipidil</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>fenofibrate</ActiveIngredient>
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							<DoseForm>Tablets</DoseForm>
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							<Side1Marking>FI</Side1Marking>
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			<brandname>Lipigem</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>61430</Austr>
				<PresentationName>Lipigem</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Gemfibrozil</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<DocumentQualifiers>
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							<Side1Marking>GL600</Side1Marking>
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							<Views>
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			</Presentations>
		</Brand><Brand>
			<brandname>Lipitor</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>168338</Austr>
				<PresentationName>Lipitor</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ATV</Side1Marking>
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							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>168341</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium</TGAIngredient>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ATV</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
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								<ImageFileName>168341-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>168342</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Scoring>unscored</Scoring>
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							<Side1Marking>ATV</Side1Marking>
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							<Views>
							<View>
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					</Versions>
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			</Presentations>
			<Presentations>
				<Austr>168344</Austr>
				<PresentationName>Lipitor</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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							<Side1Marking>ATV</Side1Marking>
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							<Views>
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							<View>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lipostat</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>118589</Austr>
				<PresentationName>Lipostat</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
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							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>118590</Austr>
				<PresentationName>Lipostat</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>118590-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>118591</Austr>
				<PresentationName>Lipostat</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>118591-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>118592</Austr>
				<PresentationName>Lipostat</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
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							<Side1Marking>80</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>118592-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Liprace</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>91378</Austr>
				<PresentationName>Liprace</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
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			<Presentations>
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				<PresentationName>Liprace</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
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							<Side2Marking></Side2Marking>
							<Views>
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					</Versions>
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			</Presentations>
		</Brand><Brand>
			<brandname>Lisinopril (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>152712</Austr>
				<PresentationName>Lisinopril AN</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>BL</Side1Marking>
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							<Views>
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			</Presentations>
			<Presentations>
				<Austr>152713</Austr>
				<PresentationName>Lisinopril AN</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>BL</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
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								<ImageFileName>152713-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>152714</Austr>
				<PresentationName>Lisinopril AN</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>BL</Side1Marking>
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							<Views>
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								<ImageFileName>152714-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lisinopril (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>213393</Austr>
				<PresentationName>APO-Lisinopril</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lisinopril dihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>06/01/2016 14:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking>BL</Side2Marking>
							<Views>
							<View>
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								<ImageFileName>213393-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>213394</Austr>
				<PresentationName>APO-Lisinopril</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lisinopril dihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking>BL</Side2Marking>
							<Views>
							<View>
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								<ImageFileName>213394-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>213395</Austr>
				<PresentationName>APO-Lisinopril </PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lisinopril dihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking>BL</Side2Marking>
							<Views>
							<View>
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								<ImageFileName>213395-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lisinopril (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>213399</Austr>
				<PresentationName>Chemmart Lisinopril </PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lisinopril dihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>10/02/2016 10:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking>BL</Side2Marking>
							<Views>
							<View>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>213400</Austr>
				<PresentationName>Chemmart Lisinopril </PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lisinopril dihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking>BL</Side2Marking>
							<Views>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>213401</Austr>
				<PresentationName>Chemmart Lisinopril </PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lisinopril dihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking>BL</Side2Marking>
							<Views>
							<View>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lisinopril (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>106502</Austr>
				<PresentationName>Lisinopril-GA</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>BL</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lisinopril (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>128154</Austr>
				<PresentationName>Lisinopril generichealth</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>128161</Austr>
				<PresentationName>Lisinopril generichealth</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/09/2011 15:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>128163</Austr>
				<PresentationName>Lisinopril generichealth</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>20</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>128163-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lisinopril (Hexal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>91384</Austr>
				<PresentationName>Lisinopril Hexal</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>91386</Austr>
				<PresentationName>Lisinopril Hexal</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
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							<Views>
							<View>
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			<Presentations>
				<Austr>91388</Austr>
				<PresentationName>Lisinopril Hexal</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 10:11</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Scoring>scored</Scoring>
							<Shape>round</Shape>
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							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
		</Brand><Brand>
			<brandname>Lisinopril (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>158100</Austr>
				<PresentationName>Lisinopril Sandoz</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lisinopril dihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 12:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>slightly red</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158100-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158101</Austr>
				<PresentationName>Lisinopril Sandoz</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lisinopril dihydrate</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>slightly red</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158108</Austr>
				<PresentationName>Lisinopril Sandoz</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lisinopril dihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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						<DateEffective>28/05/2012 12:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
							<Colour>slightly red</Colour>
							<Scoring>scored</Scoring>
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							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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								<ImageFileName>158108-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
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			</Presentations>
		</Brand><Brand>
			<brandname>Lisinopril (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>213396</Austr>
				<PresentationName>Terry White Chemists Lisinopril </PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lisinopril dihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/02/2016 11:38</DateEffective>
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							<DoseForm>Tablets</DoseForm>
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							<Shape>circular</Shape>
							<Side1Marking>5</Side1Marking>
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			</Presentations>
			<Presentations>
				<Austr>213397</Austr>
				<PresentationName>Terry White Chemists Lisinopril</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lisinopril dihydrate</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Shape>circular</Shape>
							<Side1Marking>10</Side1Marking>
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							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>213398</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lisinopril dihydrate</TGAIngredient>
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							<Views>
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			<brandname>Lithicarb</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>49625</Austr>
				<PresentationName>Lithicarb</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Lithium carbonate</TGAIngredient>
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							<Scoring>scored</Scoring>
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							<Views>
							<View>
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			</Presentations>
		</Brand><Brand>
			<brandname>Livial</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>55088</Austr>
				<PresentationName>Livial</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tibolone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<QualiferData></QualiferData>
						<DocumentName>Livial</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>tibolone</ActiveIngredient>
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							<Side1Marking>MK 2</Side1Marking>
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							<Views>
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			</Presentations>
		</Brand><Brand>
			<brandname>Livilan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>283947</Austr>
				<PresentationName>Livilan</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
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							<Side1Marking>TO 2</Side1Marking>
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							<Views>
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			<brandname>Loette</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>215494</Austr>
				<PresentationName>Loette</PresentationName>
    			<PresentionStrength>100mcg/20mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Levonorgestrel,Ethinyloestradiol</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentTypes>
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							<AvailableFormats>
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							<Views>
							<View>
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							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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			</Presentations>
		</Brand><Brand>
			<brandname>Lofenoxal</brandname>
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			<Presentations>
				<Austr>74476</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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							<Views>
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			<brandname>Logem</brandname>
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			<Presentations>
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				<PresentationName>Logem</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<VersionSequence>1</VersionSequence>
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							<PhaseItem>1</PhaseItem>
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							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
		</Brand><Brand>
			<brandname>Lorazepam (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>304306</Austr>
				<PresentationName>APO-Lorazepam</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
							<Side1Marking>1.0</Side1Marking>
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							<View>
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			<Presentations>
				<Austr>304307</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
		</Brand><Brand>
			<brandname>Lorstat</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>181404</Austr>
				<PresentationName>Lorstat</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
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			</Presentations>
			<Presentations>
				<Austr>181405</Austr>
				<PresentationName>Lorstat</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>181406</Austr>
				<PresentationName>Lorstat</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>80</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</View>
							</Views>
						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>181407</Austr>
				<PresentationName>Lorstat</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>334861</Austr>
				<PresentationName>Lorstat</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<VersionSequence>1</VersionSequence>
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						<DateEffective>20/05/2021 10:36</DateEffective>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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								<ViewLabel>C</ViewLabel>
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							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>334862</Austr>
				<PresentationName>Lorstat</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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							<DocumentType>eCMI</DocumentType>
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						<ActiveIngredient>atorvastatin calcium</ActiveIngredient>
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						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>334863</Austr>
				<PresentationName>Lorstat</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Lorstat (New Formulation)</DocumentName>
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						</DocumentTypes>
						<ActiveIngredient>atorvastatin calcium</ActiveIngredient>
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					</DocumentQualifiers>
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						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>40</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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							</View>
							</Views>
						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>334864</Austr>
				<PresentationName>Lorstat</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lorstat (New Formulation)</DocumentName>
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							<DocumentType>eCMI</DocumentType>
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								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>atorvastatin calcium</ActiveIngredient>
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						<VersionSequence>1</VersionSequence>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>80</Side1Marking>
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							<View>
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							</View>
							</Views>
						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>334865</Austr>
				<PresentationName>Lorstat</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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							<DocumentType>eCMI</DocumentType>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Side2Marking></Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>334866</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>atorvastatin calcium trihydrate</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Lorstat (New Formulation)</DocumentName>
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						<ActiveIngredient>atorvastatin calcium</ActiveIngredient>
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							<PhaseItem>1</PhaseItem>
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			<Presentations>
				<Austr>334867</Austr>
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    			<PresentionStrength>40mg</PresentionStrength>
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    			<Container>bottle</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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			<Presentations>
				<Austr>334868</Austr>
				<PresentationName>Lorstat</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lorstat (New Formulation)</DocumentName>
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							<DocumentType>eCMI</DocumentType>
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								<Format>PDF</Format>
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						<ActiveIngredient>atorvastatin calcium</ActiveIngredient>
						<ReleaseDate>2021-07-29 09:38:30.0</ReleaseDate>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/05/2021 10:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>334868-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Losec</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>63414</Austr>
				<PresentationName>Losec Tablets</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Omeprazole magnesium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>08/08/2008 11:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>10MG</Side1Marking>
							<Side2Marking>logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>63414-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>63416</Austr>
				<PresentationName>Losec Tablets</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Omeprazole magnesium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/08/2008 11:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>20MG</Side1Marking>
							<Side2Marking>logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>63416-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lovan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>54700</Austr>
				<PresentationName>Lovan</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lovan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afclovan11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fluoxetine hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-10-05 14:24:16.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>54700-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>61080</Austr>
				<PresentationName>Lovan</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lovan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afclovan11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fluoxetine hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-10-05 14:24:16.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>4400</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>61080-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lovir</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>62379</Austr>
				<PresentationName>Lovir</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 13:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>ACV</Side1Marking>
							<Side2Marking>200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62379-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Loxalate</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>119964</Austr>
				<PresentationName>Loxalate</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Escitalopram oxalate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Loxalate</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcloxal10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>escitalopram oxalate</ActiveIngredient>
						<ReleaseDate>2022-06-24 16:23:08.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/02/2010 15:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>EC 10</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>119964-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>119966</Austr>
				<PresentationName>Loxalate</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Escitalopram oxalate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Loxalate</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>escitalopram oxalate</ActiveIngredient>
						<ReleaseDate>2022-06-24 16:23:08.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/02/2010 15:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>EC 20</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>119966-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lozanoc</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>206360</Austr>
				<PresentationName>Lozanoc</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lozanoc</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ynclozan50220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>itraconazole</ActiveIngredient>
						<ReleaseDate>2020-02-28 15:18:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/09/2020 10:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>i-50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>206360-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>206361</Austr>
				<PresentationName>Lozanoc</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lozanoc</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ynclozan50220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>itraconazole</ActiveIngredient>
						<ReleaseDate>2020-02-28 15:18:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/10/2014 16:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>i-50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>206361-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>LPV</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>66510</Austr>
				<PresentationName>LPV</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Phenoxymethylpenicillin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>LPV</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>iaclpvmi11117</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>phenoxymethylpenicillin</ActiveIngredient>
						<ReleaseDate>2017-12-07 11:56:14.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/11/2008 13:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>grey and red</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>LPV250</Side1Marking>
							<Side2Marking>LPV250</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>66510-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>66511</Austr>
				<PresentationName>LPV</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Phenoxymethylpenicillin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>LPV</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>iaclpvmi11117</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>phenoxymethylpenicillin</ActiveIngredient>
						<ReleaseDate>2017-12-07 11:56:14.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/11/2008 13:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red and pink</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>LPV500</Side1Marking>
							<Side2Marking>LPV500</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>66511-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lukair</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>197283</Austr>
				<PresentationName>Lukair</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Montelukast sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lukair</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>montelukast sodium</ActiveIngredient>
						<ReleaseDate>2021-04-20 13:53:06.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/09/2014 12:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>711</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>197283-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>197284</Austr>
				<PresentationName>Lukair</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Montelukast sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lukair</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqclukai20221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>montelukast sodium</ActiveIngredient>
						<ReleaseDate>2021-04-20 13:53:06.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/03/2016 09:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>275</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>197284-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>197285</Austr>
				<PresentationName>Lukair</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Montelukast sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lukair</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqclukai20221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>montelukast sodium</ActiveIngredient>
						<ReleaseDate>2021-04-20 13:53:06.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/09/2014 12:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rounded square</Shape>
							<Side1Marking>117</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>197285-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lumin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>55272</Austr>
				<PresentationName>Lumin</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mianserin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lumin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afclumin11219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>mianserin hydrochloride</ActiveIngredient>
						<ReleaseDate>2019-12-23 13:44:39.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>MI 10</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>55272-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>55273</Austr>
				<PresentationName>Lumin</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mianserin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lumin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afclumin11219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>mianserin hydrochloride</ActiveIngredient>
						<ReleaseDate>2019-12-23 13:44:39.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>MI 20</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>55273-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lunava</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>164966</Austr>
				<PresentationName>Lunava</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>164966-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>164967</Austr>
				<PresentationName>Lunava</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>164967-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Luvox</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>57632</Austr>
				<PresentationName>Luvox</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluvoxamine maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Luvox</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocluvox20122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fluvoxamine maleate</ActiveIngredient>
						<ReleaseDate>2022-01-17 08:10:48.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/09/2014 11:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>291 291</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>57632-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>57633</Austr>
				<PresentationName>Luvox</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluvoxamine maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Luvox</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocluvox20122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fluvoxamine maleate</ActiveIngredient>
						<ReleaseDate>2022-01-17 08:10:48.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/09/2014 11:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>313 313</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>57633-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lycinate</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>94215</Austr>
				<PresentationName>Lycinate</PresentationName>
    			<PresentionStrength>600mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/04/2012 14:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>square</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>94215-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lynparza</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>288613</Austr>
				<PresentationName>Lynparza Tablets</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>olaparib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lynparza Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apclyntb10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>olaparib</ActiveIngredient>
						<ReleaseDate>2022-02-18 16:03:15.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/10/2018 11:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow to dark yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>OP 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>288613-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>288614</Austr>
				<PresentationName>Lynparza Tablets</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>olaparib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Lynparza Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apclyntb10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>olaparib</ActiveIngredient>
						<ReleaseDate>2022-02-18 16:03:15.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/10/2018 11:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green to green/grey</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>OP 150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>288614-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lypralin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>235846</Austr>
				<PresentationName>Lypralin</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/05/2018 08:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>PG</Side1Marking>
							<Side2Marking>150</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>235846-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>235863</Austr>
				<PresentationName>Lypralin</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/05/2018 08:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red opaque and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>PG</Side1Marking>
							<Side2Marking>75</Side2Marking>
							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>235874</Austr>
				<PresentationName>Lypralin</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white oqaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>PG</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>235879</Austr>
				<PresentationName>Lypralin</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red opaque and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>PG</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>235879-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lyrica</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>99469</Austr>
				<PresentationName>Lyrica</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Pregabalin</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>19/05/2009 09:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Pfizer</Side1Marking>
							<Side2Marking>PGN 25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>99469-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>99520</Austr>
				<PresentationName>Lyrica</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pregabalin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<QualiferData></QualiferData>
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						</DocumentTypes>
						<ActiveIngredient>pregabalin</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/09/2008 14:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Pfizer</Side1Marking>
							<Side2Marking>PGN 75</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>99520-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>99528</Austr>
				<PresentationName>Lyrica</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pregabalin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Lyrica</DocumentName>
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						<ActiveIngredient>pregabalin</ActiveIngredient>
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				</Documents>
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						<VersionSequence>1</VersionSequence>
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						<DateEffective>22/09/2011 15:44</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Pfizer</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>99537</Austr>
				<PresentationName>Lyrica</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pregabalin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<ActiveIngredient>pregabalin</ActiveIngredient>
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				</Documents>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Pfizer</Side1Marking>
							<Side2Marking>PGN 300</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>99537-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Lyzalon</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>338470</Austr>
				<PresentationName>Lyzalon (New Formulation)</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsule</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Lyzalon (New Formulation)</DocumentName>
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						<ActiveIngredient>pregabalin</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/06/2021 14:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light peach and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>MYLAN PG300</Side1Marking>
							<Side2Marking>MYLAN PG300</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>338471</Austr>
				<PresentationName>Lyzalon (New Formulation)</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsule</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Lyzalon (New Formulation)</DocumentName>
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						<ActiveIngredient>pregabalin</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>30/06/2021 14:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light peach and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>MYLAN PG25</Side1Marking>
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							<Views>
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								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>338472</Austr>
				<PresentationName>Lyzalon (New Formulation)</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Capsule</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Lyzalon (New Formulation)</DocumentName>
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						<ActiveIngredient>pregabalin</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>30/06/2021 14:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light peach</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>MYLAN PG75</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>338473</Austr>
				<PresentationName>Lyzalon (New Formulation)</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsule</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Lyzalon (New Formulation)</DocumentName>
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							<AvailableFormats>
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						</DocumentTypes>
						<ActiveIngredient>pregabalin</ActiveIngredient>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light peach and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>MYLAN PG150</Side1Marking>
							<Side2Marking>MYLAN PG150</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
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			</Presentations>
		</Brand><Brand>
			<brandname>Macrodantin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>60064</Austr>
				<PresentationName>Macrodantin</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Nitrofurantoin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Macrodantin</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
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						</DocumentTypes>
						<ActiveIngredient>nitrofurantoin</ActiveIngredient>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>EATON 008</Side1Marking>
							<Side2Marking>EATON 008</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>60064-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>60065</Austr>
				<PresentationName>Macrodantin</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Nitrofurantoin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Macrodantin</DocumentName>
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						<ActiveIngredient>nitrofurantoin</ActiveIngredient>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow</Colour>
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							<Shape></Shape>
							<Side1Marking>EATON 009</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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		</Brand><Brand>
			<brandname>Madeline</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>202833</Austr>
				<PresentationName>Madeline</PresentationName>
    			<PresentionStrength>150mcg/30mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ethinyloestradiol,Desogestrel</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/09/2014 11:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>MI</Side1Marking>
							<Side2Marking>7</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>202833-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>202833-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Madopar</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>13742</Austr>
				<PresentationName>Madopar</PresentationName>
    			<PresentionStrength>200mg/50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Benserazide hydrochloride,Levodopa</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Madopar</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>rocmadop11121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levodopa with benserazide</ActiveIngredient>
						<ReleaseDate>2021-11-25 11:43:53.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/11/2012 13:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>powder blue and caramel</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>ROCHE</Side1Marking>
							<Side2Marking>ROCHE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>13742-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>13743</Austr>
				<PresentationName>Madopar HBS</PresentationName>
    			<PresentionStrength>100mg/25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Levodopa,Benserazide hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Madopar</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>rocmadop11121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levodopa with benserazide</ActiveIngredient>
						<ReleaseDate>2021-11-25 11:43:53.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 15:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>dark green/light blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>ROCHE</Side1Marking>
							<Side2Marking>ROCHE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>13743-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>13744</Austr>
				<PresentationName>Madopar</PresentationName>
    			<PresentionStrength>50mg/12.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Levodopa,Benserazide hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Madopar</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>rocmadop11121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levodopa with benserazide</ActiveIngredient>
						<ReleaseDate>2021-11-25 11:43:53.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/11/2012 13:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>powder blue and light grey</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>ROCHE</Side1Marking>
							<Side2Marking>ROCHE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>13744-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>13745</Austr>
				<PresentationName>Madopar</PresentationName>
    			<PresentionStrength>200mg/50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Levodopa,Benserazide hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Madopar</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>rocmadop11121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levodopa with benserazide</ActiveIngredient>
						<ReleaseDate>2021-11-25 11:43:53.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/06/2018 10:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale red</Colour>
							<Scoring>scored</Scoring>
							<Shape>cylindrical</Shape>
							<Side1Marking>RO C HE hexagon</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>13745-A01-02-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>13745-B01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>13746</Austr>
				<PresentationName>Madopar</PresentationName>
    			<PresentionStrength>100mg/25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Benserazide hydrochloride,Levodopa</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Madopar</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>rocmadop11121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levodopa with benserazide</ActiveIngredient>
						<ReleaseDate>2021-11-25 11:43:53.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/11/2012 13:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>powder blue and flesh</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>ROCHE</Side1Marking>
							<Side2Marking>ROCHE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>13746-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>43517</Austr>
				<PresentationName>Madopar</PresentationName>
    			<PresentionStrength>100mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Benserazide,Levodopa</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Madopar</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>rocmadop11121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levodopa with benserazide</ActiveIngredient>
						<ReleaseDate>2021-11-25 11:43:53.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/09/2008 16:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale red</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>43517-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>59576</Austr>
				<PresentationName>Madopar Rapid</PresentationName>
    			<PresentionStrength>100mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Levodopa,Benserazide hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Madopar</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>rocmadop11121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levodopa with benserazide</ActiveIngredient>
						<ReleaseDate>2021-11-25 11:43:53.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/09/2008 16:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROCHE 125</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>59576-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>59577</Austr>
				<PresentationName>Madopar Rapid</PresentationName>
    			<PresentionStrength>50mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Benserazide hydrochloride,Levodopa</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Madopar</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>rocmadop11121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levodopa with benserazide</ActiveIngredient>
						<ReleaseDate>2021-11-25 11:43:53.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 14:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROCHE 62.5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>59577-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Magnesium (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>226998</Austr>
				<PresentationName>Pharmacy Action Magnesium High Dose 1-a-Day</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/05/2017 17:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>226998-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Malarone</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>61100</Austr>
				<PresentationName>Malarone</PresentationName>
    			<PresentionStrength>250mg/100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Proguanil hydrochloride,Atovaquone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Malarone</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gwcmalar11215</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>atovaquone with proguanil hydrochloride</ActiveIngredient>
						<ReleaseDate>2016-03-15 15:34:36.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 15:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>GX CM3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>61100-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>92855</Austr>
				<PresentationName>Malarone</PresentationName>
    			<PresentionStrength>62.5mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Proguanil hydrochloride,Atovaquone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Malarone</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gwcmalar11215</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>atovaquone with proguanil hydrochloride</ActiveIngredient>
						<ReleaseDate>2016-03-15 15:34:36.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 15:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>GX CG7</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>92855-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Malean</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>196485</Austr>
				<PresentationName>Malean</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
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							<Side2Marking></Side2Marking>
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							<View>
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			</Presentations>
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			<brandname>Maosig</brandname>
			<isamtbrand>true</isamtbrand>
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							<Side2Marking></Side2Marking>
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								<ImageFileName>78245-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
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			<brandname>Marevan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>12511</Austr>
				<PresentationName>Marevan</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
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						<DateEffective>27/04/2012 14:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<DoseForm>Tablets</DoseForm>
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			<Presentations>
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				<PresentationName>Marevan</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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		</Brand><Brand>
			<brandname>Marvelon</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>42894</Austr>
				<PresentationName>Marvelon 28</PresentationName>
    			<PresentionStrength>30mcg/150mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>KH 2</Side1Marking>
							<Side2Marking>Square</Side2Marking>
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								<ImageFileName>42894-C02-01-BL600.jpg</ImageFileName>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>69076</Austr>
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    			<PresentationForm>Wafers</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rizatriptan benzoate</TGAIngredient>
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		</Brand><Brand>
			<brandname>Maxamox</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>76050</Austr>
				<PresentationName>Maxamox</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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			<brandname>Maxiclear Cold and Flu Relief</brandname>
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			<brandname>Maxiclear Sinus &amp; Pain Relief</brandname>
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				<Austr>167173</Austr>
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			<brandname>Maxiclear Sinus Relief</brandname>
			<isamtbrand>true</isamtbrand>
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    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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			<Presentations>
				<Austr>127503</Austr>
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			<Presentations>
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			<Presentations>
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    			<Container>blister pack</Container>
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    			<Container>blister pack</Container>
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			<Presentations>
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							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>127414</Austr>
				<PresentationName>Meloxibell</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/09/2011 15:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127414-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Meloxicam (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>127415</Austr>
				<PresentationName>Pharmacor Meloxicam</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/09/2009 15:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127415-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127416</Austr>
				<PresentationName>Pharmacor Meloxicam</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/09/2009 15:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127416-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Meloxicam (Ranbaxy)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>127417</Austr>
				<PresentationName>Meloxicam Ranbaxy</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/02/2009 13:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127417-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127418</Austr>
				<PresentationName>Meloxicam Ranbaxy</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/02/2009 13:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127418-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Meloxicam (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>199661</Austr>
				<PresentationName>Meloxicam Sandoz</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Meloxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/07/2016 12:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199661-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199662</Austr>
				<PresentationName>Meloxicam Sandoz</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Meloxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/07/2016 12:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light green and light yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199662-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>288943</Austr>
				<PresentationName>Meloxicam Sandoz</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>10/01/2018 11:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>288943-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>288944</Austr>
				<PresentationName>Meloxicam Sandoz</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/01/2018 11:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>288944-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Meloxicam (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>127501</Austr>
				<PresentationName>Terry White Chemists Meloxicam</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Meloxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/11/2012 14:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pastel yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>7.5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127501-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127505</Austr>
				<PresentationName>Terry White Chemists Meloxicam</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Meloxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
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						<DateEffective>07/11/2012 14:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pastel yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>MEL 15</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127505-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>181204</Austr>
				<PresentationName>Terry White Chemists Meloxicam Capsules</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Meloxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/06/2012 13:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>181204-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>181205</Austr>
				<PresentationName>Terry White Chemists Meloxicam Capsules</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Meloxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light green and light yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>181205-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Memantine Hydrochloride (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>159582</Austr>
				<PresentationName>APO-Memantine</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Memantine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<DateEffective>23/03/2011 10:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>peanut-shaped</Shape>
							<Side1Marking>MEM 10</Side1Marking>
							<Side2Marking>APO APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159582-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>207782</Austr>
				<PresentationName>APO-Memantine</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Memantine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MEM 20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>207782-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Memantine Hydrochloride (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>168425</Austr>
				<PresentationName>Memantine generichealth</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>10</Side1Marking>
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							<Views>
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			</Presentations>
		</Brand><Brand>
			<brandname>Menevit</brandname>
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			<Presentations>
				<Austr>141364</Austr>
				<PresentationName>Menevit</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
				<Austr>10109</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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							<Side1Marking>MERSYNDOL 008</Side1Marking>
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			<Presentations>
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			<Presentations>
				<Austr>59985</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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			<brandname>Mesalazine (Takeda)</brandname>
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			<Presentations>
				<Austr>316122</Austr>
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			<Presentations>
				<Austr>289132</Austr>
				<PresentationName>Mesasal</PresentationName>
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			<Presentations>
				<Austr>13747</Austr>
				<PresentationName>Mestinon</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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				<Documents>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
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				<Documents>
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						<ActiveIngredient>phentermine</ActiveIngredient>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/03/2010 09:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque light grey and opaque green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>METERMINE 15</Side1Marking>
							<Side2Marking>METERMINE 15</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101828-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101829</Austr>
				<PresentationName>Metermine</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Phentermine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<ActiveIngredient>phentermine</ActiveIngredient>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>08/03/2010 09:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque grey and opaque reddish brown</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>METERMINE 30</Side1Marking>
							<Side2Marking>METERMINE 30</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101829-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101830</Austr>
				<PresentationName>Metermine</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Phentermine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<QualiferData></QualiferData>
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								<Format>PDF</Format>
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						<ActiveIngredient>phentermine</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/03/2010 09:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque light grey and opaque orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>METERMINE 40</Side1Marking>
							<Side2Marking>METERMINE 40</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101830-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Metex XR</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>232639</Austr>
				<PresentationName>Metex XR</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>XR 1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>232639-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>232661</Austr>
				<PresentationName>Metex XR</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/06/2019 16:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>XR 500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>232661-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Metformin Hydrochloride (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>180431</Austr>
				<PresentationName>Metformin AN</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>6 2</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>180431-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>180434</Austr>
				<PresentationName>Metformin AN</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>60</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>180434-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>180436</Austr>
				<PresentationName>Metformin AN</PresentationName>
    			<PresentionStrength>850mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>61</Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>180436-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>180436-B01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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		</Brand><Brand>
			<brandname>Metformin Hydrochloride (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>197407</Austr>
				<PresentationName>Metformin XR APOTEX</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-10-21 00:00:00'}</WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 12:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>XR500</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>197407-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
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			</Presentations>
			<Presentations>
				<Austr>218272</Austr>
				<PresentationName>Metformin XR APOTEX</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 12:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>MXR1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>218272-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>281210</Austr>
				<PresentationName>APO-Metformin XR </PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/11/2017 11:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>XR 1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>281210-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>281211</Austr>
				<PresentationName>APO-Metformin XR</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>16/11/2017 11:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>XR 500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>281211-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
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			</Presentations>
			<Presentations>
				<Austr>310117</Austr>
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    			<PresentionStrength>850mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>23/06/2022 11:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>850</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>310117-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>310117-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>310118</Austr>
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    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2022 11:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>310118-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
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				</Images>
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		</Brand><Brand>
			<brandname>Metformin Hydrochloride (Blooms The Chemist)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>278175</Austr>
				<PresentationName>Blooms The Chemist Metformin XR</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 12:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>XR 1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>278175-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>278176</Austr>
				<PresentationName>Blooms The Chemist Metformin XR</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 12:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>XR 500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>278176-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Metformin Hydrochloride (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>174817</Austr>
				<PresentationName>Chemmart Metformin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/06/2012 11:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>174817-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>174818</Austr>
				<PresentationName>Chemmart Metformin</PresentationName>
    			<PresentionStrength>850mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/06/2012 11:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>850</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>174818-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>174818-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>176510</Austr>
				<PresentationName>Chemmart Metformin</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/05/2012 10:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>176510-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>197405</Austr>
				<PresentationName>Chemmart Metformin XR</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>XR500</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>197405-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>278177</Austr>
				<PresentationName>Chemmart Metformin XR</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/09/2018 12:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>XR 1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>278177-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>278178</Austr>
				<PresentationName>Chemmart Metformin XR</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/09/2018 12:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>XR 500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>278178-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>78616</Austr>
				<PresentationName>Chemmart Metformin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/08/2008 09:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>M500</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>78616-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>78616-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>78620</Austr>
				<PresentationName>Chemmart Metformin</PresentationName>
    			<PresentionStrength>850mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/08/2008 09:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>850</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>78620-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Metformin Hydrochloride (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>147411</Austr>
				<PresentationName>Metformin-GA</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 14:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>147411-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>147643</Austr>
				<PresentationName>Metformin-GA</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 14:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>147643-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>147644</Austr>
				<PresentationName>Metformin-GA</PresentationName>
    			<PresentionStrength>850mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 14:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>850</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>147644-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Metformin Hydrochloride (Genepharm)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>108666</Austr>
				<PresentationName>Metformin Hydrochloride</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 12:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>108666-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>108667</Austr>
				<PresentationName>Metformin Hydrochloride</PresentationName>
    			<PresentionStrength>850mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 12:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>850</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>108667-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>108667-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Metformin Hydrochloride (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>164469</Austr>
				<PresentationName>Metformin generichealth 1000</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/10/2012 12:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>164469-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Metformin Hydrochloride (GenRx)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>78617</Austr>
				<PresentationName>GenRx Metformin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/07/2008 14:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>M500</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>78617-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>78617-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>78621</Austr>
				<PresentationName>GenRx Metformin</PresentationName>
    			<PresentionStrength>850mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/07/2008 14:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>850</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>78621-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Metformin Hydrochloride (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>130319</Austr>
				<PresentationName>Pharmacor Metformin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/10/2010 15:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>130319-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>130320</Austr>
				<PresentationName>Pharmacor Metformin</PresentationName>
    			<PresentionStrength>850mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/10/2010 15:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>850</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>130320-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>130320-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158538</Austr>
				<PresentationName>Pharmacor Metformin</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/10/2010 15:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158538-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Metformin Hydrochloride (Ranbaxy)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>142876</Austr>
				<PresentationName>Metformin Ranbaxy</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>142876-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>142884</Austr>
				<PresentationName>Metformin Ranbaxy</PresentationName>
    			<PresentionStrength>850mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>850</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>142884-A01-02-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>142884-B01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>170439</Austr>
				<PresentationName>Metformin Ranbaxy</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 15:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>170439-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Metformin Hydrochloride (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>123665</Austr>
				<PresentationName>Metformin Sandoz</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/09/2008 18:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>M 1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>123665-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>123673</Austr>
				<PresentationName>Metformin Sandoz</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/04/2011 15:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>M 1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>123673-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>125661</Austr>
				<PresentationName>Metformin Sandoz</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/04/2012 17:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>125661-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>125662</Austr>
				<PresentationName>Metformin Sandoz</PresentationName>
    			<PresentionStrength>850mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/04/2012 17:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>850</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>125662-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>125662-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>148268</Austr>
				<PresentationName>Metformin Sandoz</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/10/2010 13:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>148268-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Metformin Hydrochloride (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>174819</Austr>
				<PresentationName>Terry White Chemists Metformin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>18/06/2012 12:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>174819-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>174820</Austr>
				<PresentationName>Terry White Chemists Metformin</PresentationName>
    			<PresentionStrength>850mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>18/06/2012 12:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>850</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>174820-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>174820-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>176511</Austr>
				<PresentationName>Terry White Chemists Metformin</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/05/2012 10:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>176511-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>197406</Austr>
				<PresentationName>Terry White Chemists Metformin XR</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>XR500</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>197406-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>278179</Austr>
				<PresentationName>Terry White Chemists Metformin XR</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/09/2018 12:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>XR 1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>278179-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>278180</Austr>
				<PresentationName>Terry White Chemists Metformin XR</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/09/2018 12:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>XR 500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>278180-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>78614</Austr>
				<PresentationName>Terry White Chemists Metformin</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/08/2008 09:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>M500</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>78614-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>78614-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>78618</Austr>
				<PresentationName>Terry White Chemists Metformin</PresentationName>
    			<PresentionStrength>850mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/08/2008 09:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>850</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>78618-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Methoblastin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>15417</Austr>
				<PresentationName>Methoblastin</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Methotrexate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Methoblastin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcmetht10422</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>methotrexate</ActiveIngredient>
						<ReleaseDate>2022-05-06 12:54:00.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/04/2012 14:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>M 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>15417-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>15418</Austr>
				<PresentationName>Methoblastin</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Methotrexate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Methoblastin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>methotrexate</ActiveIngredient>
						<ReleaseDate>2022-05-06 12:54:00.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/12/2009 13:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring></Scoring>
							<Shape>round</Shape>
							<Side1Marking>M 2.5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>15418-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Methylphenidate (Arrotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>344270</Austr>
				<PresentationName>Methylphenidate XR ARX</PresentationName>
    			<PresentionStrength>27mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Methylphenidate XR ARX</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>methylphenidate hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-03-15 14:54:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>grey</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>2393</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>344270-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>344274</Austr>
				<PresentationName>Methylphenidate XR ARX</PresentationName>
    			<PresentionStrength>18mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Methylphenidate XR ARX</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcmearx10322</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>methylphenidate hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-03-15 14:54:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>2392</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>344274-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>344275</Austr>
				<PresentationName>Methylphenidate XR ARX</PresentationName>
    			<PresentionStrength>54mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Methylphenidate XR ARX</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcmearx10322</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>methylphenidate hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-03-15 14:54:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brownish-red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>2395</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>344275-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>344277</Austr>
				<PresentationName>Methylphenidate XR ARX</PresentationName>
    			<PresentionStrength>36mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Methylphenidate XR ARX</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcmearx10322</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>methylphenidate hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-03-15 14:54:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>2394</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>344277-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Methylphenidate (Teva)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>370899</Austr>
				<PresentationName>Methylphenidate-Teva XR</PresentationName>
    			<PresentionStrength>54mg</PresentionStrength>
    			<PresentationForm>Tablets </PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>methylphenidate hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Methylphenidate-Teva XR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>methylphenidate hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-03-15 14:54:19.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brownish-red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>2395</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>370899-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>370900</Austr>
				<PresentationName>Methylphenidate-Teva XR</PresentationName>
    			<PresentionStrength>36mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>methylphenidate hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Methylphenidate-Teva XR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>methylphenidate hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-03-15 14:54:19.0</ReleaseDate>
					</DocumentQualifiers>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>2394</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>370900-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>370911</Austr>
				<PresentationName>Methylphenidate-Teva XR</PresentationName>
    			<PresentionStrength>27mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>methylphenidate hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Methylphenidate-Teva XR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
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						</DocumentTypes>
						<ActiveIngredient>methylphenidate hydrochloride</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>28/09/2022 22:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>grey</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>2393</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>370911-C01-01-BL600.jpg</ImageFileName>
							</View>
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			<Presentations>
				<Austr>370912</Austr>
				<PresentationName>Methylphenidate-Teva XR</PresentationName>
    			<PresentionStrength>18mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>methylphenidate hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
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						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>methylphenidate hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-03-15 14:54:19.0</ReleaseDate>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/09/2022 22:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>2392</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>370912-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Metoclopramide (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>196502</Austr>
				<PresentationName>APO-Metoclopramide</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metoclopramide hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/09/2014 11:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>196502-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Metoclopramide Hydrochloride (Actavis)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>196508</Austr>
				<PresentationName>Metoclopramide Actavis</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 14:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>196508-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Metoclopramide Hydrochloride (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>196492</Austr>
				<PresentationName>Metoclopramide AN</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>196492-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Metomax</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>121343</Austr>
				<PresentationName>Metomax</PresentationName>
    			<PresentionStrength> 5mg/500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>metoclopramide hydrochloride monohydrate,paracetamol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Metomax</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green and yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>&#945;</Side1Marking>
							<Side2Marking>P500/M5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121343-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Metopirone</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>11043</Austr>
				<PresentationName>Metopirone</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Metyrapone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/12/2008 11:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>cream</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>L N</Side1Marking>
							<Side2Marking>CIBA</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>11043-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Metoprolol Tartrate (Actavis)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>192777</Austr>
				<PresentationName>Metoprolol Actavis</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 14:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>B L</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192777-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>192782</Austr>
				<PresentationName>Metoprolol Actavis</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 14:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>B L</Side1Marking>
							<Side2Marking>50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192782-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Metoprolol Tartrate (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>192765</Austr>
				<PresentationName>Metoprolol AN</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>B L</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192765-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>192767</Austr>
				<PresentationName>Metoprolol AN</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>B L</Side1Marking>
							<Side2Marking>50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192767-C01-01-BL600.jpg</ImageFileName>
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		</Brand><Brand>
			<brandname>Metoprolol Tartrate (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>192766</Austr>
				<PresentationName>APO-Metoprolol</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metoprolol tartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/09/2018 09:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192766-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>192772</Austr>
				<PresentationName>APO-Metoprolol</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metoprolol tartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/09/2018 09:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192772-C01-02-BL600.jpg</ImageFileName>
							</View>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Metoprolol Tartrate (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>210512</Austr>
				<PresentationName>Chemmart Metoprolol</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metoprolol tartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/09/2018 12:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
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							<Side2Marking></Side2Marking>
							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>210513</Austr>
				<PresentationName>Chemmart Metoprolol</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metoprolol tartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
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						<DateEffective>26/09/2018 12:40</DateEffective>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>210513-C01-02-BL600.jpg</ImageFileName>
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				</Images>
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		</Brand><Brand>
			<brandname>Metoprolol Tartrate (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>62560</Austr>
				<PresentationName>Metoprolol Sandoz</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metoprolol tartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<DateEffective>25/09/2008 13:55</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
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			<isamtbrand>true</isamtbrand>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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				<Austr>155172</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient>telmisartan,hydrochlorothiazide</TGAIngredient>
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						<QualiferData></QualiferData>
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			</Presentations>
			<Presentations>
				<Austr>82416</Austr>
				<PresentationName>Micardis Plus</PresentationName>
    			<PresentionStrength>40/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>telmisartan,hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<AvailableFormats>
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			</Presentations>
			<Presentations>
				<Austr>82418</Austr>
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    			<PresentionStrength>80/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>telmisartan,hydrochlorothiazide</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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			<brandname>Microgynon</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10692</Austr>
				<PresentationName>Microgynon 30</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>10693</Austr>
				<PresentationName>Microgynon 30 ED</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
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							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>10695</Austr>
				<PresentationName>Microgynon 50 ED</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Colour>ochre</Colour>
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							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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							<View>
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			</Presentations>
			<Presentations>
				<Austr>63484</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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		</Brand><Brand>
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			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>63486</Austr>
				<PresentationName>Microlevlen ED</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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							<View>
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			<brandname>Microlut</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10696</Austr>
				<PresentationName>Microlut</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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			<brandname>Micronelle 20 ED</brandname>
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			<Presentations>
				<Austr>211154</Austr>
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    			<PresentionStrength>20mcg/100mcg</PresentionStrength>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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						<VersionSequence>1</VersionSequence>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MT2</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>205149-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>205150</Austr>
				<PresentationName>Minax XL</PresentationName>
    			<PresentionStrength>190mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metoprolol succinate</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Minax XL</DocumentName>
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							<DocumentType>eCMI</DocumentType>
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								<Format>PDF</Format>
								<Filename>afcminxl10120</Filename>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MT4</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>205150-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>205151</Austr>
				<PresentationName>Minax XL</PresentationName>
    			<PresentionStrength>23.75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metoprolol succinate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Minax XL</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/03/2018 13:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>MT1</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>205151-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>34408</Austr>
				<PresentationName>Minax</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Metoprolol tartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Minax</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcminax10520</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>metoprolol tartrate</ActiveIngredient>
						<ReleaseDate>2020-06-02 11:30:19.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ML 50</Side1Marking>
							<Side2Marking>&#945;</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>34408-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>34410</Austr>
				<PresentationName>Minax</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Metoprolol tartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Minax</DocumentName>
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							<DocumentType>eCMI</DocumentType>
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								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>metoprolol tartrate</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ML 100</Side1Marking>
							<Side2Marking>&#945;</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>34410-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Minidiab</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>15421</Austr>
				<PresentationName>Minidiab</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Glipizide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Minidiab</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
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						<ActiveIngredient>glipizide</ActiveIngredient>
						<ReleaseDate>2019-12-09 11:30:09.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/09/2011 15:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>round</Shape>
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							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>15421-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Minipress</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10756</Austr>
				<PresentationName>Minipress</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Prazosin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Minipress</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>prazosin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-03-10 13:06:11.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/09/2011 15:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>MNP 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10756-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>10757</Austr>
				<PresentationName>Minipress</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Prazosin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Minipress</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>prazosin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-03-10 13:06:11.0</ReleaseDate>
					</DocumentQualifiers>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/09/2008 11:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>MNP 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10757-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>10758</Austr>
				<PresentationName>Minipress</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Prazosin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Minipress</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>prazosin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-03-10 13:06:11.0</ReleaseDate>
					</DocumentQualifiers>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/09/2008 11:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>diamond-shaped</Shape>
							<Side1Marking>MNP 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10758-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Minirin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>121721</Austr>
				<PresentationName>Minirin Melt</PresentationName>
    			<PresentionStrength>120mcg</PresentionStrength>
    			<PresentationForm>Wafers</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Desmopressin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Minirin Melt</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>desmopressin</ActiveIngredient>
						<ReleaseDate>2015-09-30 13:58:44.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/05/2009 13:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Wafers</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape>round</Shape>
							<Side1Marking>two drop shaped figures</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>121721-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>121721-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121722</Austr>
				<PresentationName>Minirin Melt</PresentationName>
    			<PresentionStrength>240mcg</PresentionStrength>
    			<PresentationForm>Wafers</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Desmopressin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Minirin Melt</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>desmopressin</ActiveIngredient>
						<ReleaseDate>2015-09-30 13:58:44.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/09/2011 14:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Wafers</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape>round</Shape>
							<Side1Marking>three drop shaped figures</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>121722-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>121722-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>93731</Austr>
				<PresentationName>Minirin Tablets</PresentationName>
    			<PresentionStrength>200mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Desmopressin acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Minirin Tablets</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>desmopressin acetate</ActiveIngredient>
						<ReleaseDate>2019-07-31 15:49:27.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>17/09/2008 14:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>0.2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>93731-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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			</Presentations>
		</Brand><Brand>
			<brandname>Minomycin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>47054</Austr>
				<PresentationName>Minomycin</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/04/2012 14:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>M50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>47054-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Minulet</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>217121</Austr>
				<PresentationName>Minulet</PresentationName>
    			<PresentionStrength>75mcg/30mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ethinyloestradiol,Gestodene</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Minulet</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcminut10120</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>gestodene with ethinylestradiol</ActiveIngredient>
						<ReleaseDate>2020-01-16 10:45:30.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>02/05/2017 10:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>217121-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>217121-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>296803</Austr>
				<PresentationName>Minulet</PresentationName>
    			<PresentionStrength>75mcg/30mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gestodene,ethinylestradiol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Minulet</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcminut10120</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>gestodene with ethinylestradiol</ActiveIngredient>
						<ReleaseDate>2020-01-16 10:45:30.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/03/2020 12:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>296803-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>296803-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>47377</Austr>
				<PresentationName>Minulet</PresentationName>
    			<PresentionStrength>75mcg/30mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ethinyloestradiol,Gestodene</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/09/2011 15:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>47377-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>47377-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Mirtanza</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>183376</Austr>
				<PresentationName>Mirtanza</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/08/2020 13:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>0 8</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183376-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183377</Austr>
				<PresentationName>Mirtanza</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/08/2020 15:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish brown</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>0 9</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183377-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183394</Austr>
				<PresentationName>Mirtanza</PresentationName>
    			<PresentionStrength>45mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/08/2020 15:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183394-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183404</Austr>
				<PresentationName>Mirtanza ODT</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2022 09:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>36</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183404-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183405</Austr>
				<PresentationName>Mirtanza ODT</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2022 09:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>37</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183405-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183406</Austr>
				<PresentationName>Mirtanza ODT</PresentationName>
    			<PresentionStrength>45mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2022 09:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>38</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183406-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Mirtazapine (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>183398</Austr>
				<PresentationName>Mirtazapine AN</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>0 8</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183398-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183399</Austr>
				<PresentationName>Mirtazapine AN</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/09/2017 09:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish brown</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>0 9</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183399-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Mirtazapine (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>127666</Austr>
				<PresentationName>APO-Mirtazapine</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MI 15</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127666-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127677</Austr>
				<PresentationName>APO-Mirtazapine</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets </PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MI 30</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127677-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127678</Austr>
				<PresentationName>APO-Mirtazapine</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MI 30</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127678-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127684</Austr>
				<PresentationName>APO-Mirtazapine</PresentationName>
    			<PresentionStrength>45mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MI-45</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127684-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127685</Austr>
				<PresentationName>APO-Mirtazapine</PresentationName>
    			<PresentionStrength>45mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/05/2012 11:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MI-45</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127685-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Mirtazapine (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>127670</Austr>
				<PresentationName>Chemmart Mirtazapine</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/11/2015 13:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MI 15</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127670-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127681</Austr>
				<PresentationName>Chemmart Mirtazapine</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/08/2008 09:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MI 30</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127681-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127698</Austr>
				<PresentationName>Chemmart Mirtazapine</PresentationName>
    			<PresentionStrength>45mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/05/2012 10:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MI-45</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127698-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Mirtazapine (Generic Health)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>191019</Austr>
				<PresentationName>Mirtazapine GH</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>191019-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>191020</Austr>
				<PresentationName>Mirtazapine GH</PresentationName>
    			<PresentionStrength>45mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>191020-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Mirtazapine (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>117156</Austr>
				<PresentationName>Mirtazapine Sandoz</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 15:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>117156-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>117157</Austr>
				<PresentationName>Mirtazapine Sandoz</PresentationName>
    			<PresentionStrength>45mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 15:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>117157-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183401</Austr>
				<PresentationName>Mirtazapine Sandoz ODT</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/08/2014 17:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>36</Side1Marking>
							<Side2Marking>A</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183401-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183402</Austr>
				<PresentationName>Mirtazapine Sandoz ODT</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/08/2014 16:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>37</Side1Marking>
							<Side2Marking>A</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183402-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183403</Austr>
				<PresentationName>Mirtazapine Sandoz ODT</PresentationName>
    			<PresentionStrength>45mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/08/2014 16:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>38</Side1Marking>
							<Side2Marking>A</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183403-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Mirtazapine (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>127673</Austr>
				<PresentationName>Terry White Chemists Mirtazapine</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/11/2015 13:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MI 15</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127673-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127683</Austr>
				<PresentationName>Terry White Chemists Mirtazapine</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/08/2008 09:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MI 30</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127683-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127699</Austr>
				<PresentationName>Terry White Chemists Mirtazapine</PresentationName>
    			<PresentionStrength>45mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mirtazapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/05/2012 10:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MI-45</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127699-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Mizart</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>230974</Austr>
				<PresentationName>Mizart</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Telmisartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Mizart</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcmiznt11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>telmisartan</ActiveIngredient>
						<ReleaseDate>2022-10-10 09:56:20.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/06/2021 14:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L203</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>230974-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>230975</Austr>
				<PresentationName>Mizart</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Telmisartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Mizart</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcmiznt11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>telmisartan</ActiveIngredient>
						<ReleaseDate>2022-10-10 09:56:20.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/06/2021 14:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L204</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>230975-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Mizart HCT</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>246472</Austr>
				<PresentationName>Mizart HCT</PresentationName>
    			<PresentionStrength>40/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Telmisartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Mizart HCT (New)</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcmizhn11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>telmisartan with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2022-10-26 11:52:03.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/10/2020 13:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled and white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L199</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>246472-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>246473</Austr>
				<PresentationName>Mizart HCT</PresentationName>
    			<PresentionStrength>80/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Telmisartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Mizart HCT (New)</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcmizhn11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>telmisartan with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2022-10-26 11:52:03.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/10/2020 13:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled and white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>246473-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>246474</Austr>
				<PresentationName>Mizart HCT</PresentationName>
    			<PresentionStrength>80/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Telmisartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Mizart HCT (New)</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcmizhn11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>telmisartan with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2022-10-26 11:52:03.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2020 11:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow mottled and white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L201</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>246474-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Mobic</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>77694</Austr>
				<PresentationName>Mobic</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>meloxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Mobic</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>bycmobic11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>meloxicam</ActiveIngredient>
						<ReleaseDate>2021-10-13 19:00:58.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/01/2010 09:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pastel yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>59D 59D</Side1Marking>
							<Side2Marking>Company Logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>77694-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>77695</Austr>
				<PresentationName>Mobic</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>meloxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Mobic</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>bycmobic11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>meloxicam</ActiveIngredient>
						<ReleaseDate>2021-10-13 19:00:58.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/01/2010 09:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pastel yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>77C 77C</Side1Marking>
							<Side2Marking>Company Logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>77695-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>77698</Austr>
				<PresentationName>Mobic</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>meloxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Mobic</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>bycmobic11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>meloxicam</ActiveIngredient>
						<ReleaseDate>2021-10-13 19:00:58.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/01/2010 09:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>pale green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>77698-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>77699</Austr>
				<PresentationName>Mobic</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>meloxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Mobic</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>bycmobic11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>meloxicam</ActiveIngredient>
						<ReleaseDate>2021-10-13 19:00:58.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/02/2010 14:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>pale yellow/pale green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>77699-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Mobilis</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>52201</Austr>
				<PresentationName>Mobilis</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Piroxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Mobilis</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcmibol10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>piroxicam</ActiveIngredient>
						<ReleaseDate>2022-02-25 11:00:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>brown and ivory</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>&#945;</Side1Marking>
							<Side2Marking>PM 10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>52201-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>52202</Austr>
				<PresentationName>Mobilis</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Piroxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Mobilis</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcmibol10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>piroxicam</ActiveIngredient>
						<ReleaseDate>2022-02-25 11:00:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light grey</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>&#945;</Side1Marking>
							<Side2Marking>PM 20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>52202-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>53282</Austr>
				<PresentationName>Mobilis D</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Piroxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Mobilis</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcmibol10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>piroxicam</ActiveIngredient>
						<ReleaseDate>2022-02-25 11:00:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/12/2010 11:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>D Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>53282-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>53284</Austr>
				<PresentationName>Mobilis D</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Piroxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Mobilis</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcmibol10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>piroxicam</ActiveIngredient>
						<ReleaseDate>2022-02-25 11:00:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/12/2010 11:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>D Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>53284-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
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			</Presentations>
		</Brand><Brand>
			<brandname>Moclobemide (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>73831</Austr>
				<PresentationName>APO-Moclobemide</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Moclobemide</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>06/08/2008 08:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>APO 150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73831-C01-01-BL600.jpg</ImageFileName>
							</View>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>73835</Austr>
				<PresentationName>APO-Moclobemide</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Moclobemide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/08/2008 08:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>APO 300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73835-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Moclobemide (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>76934</Austr>
				<PresentationName>Moclobemide Sandoz</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Moclobemide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 16:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>76934-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>76935</Austr>
				<PresentationName>Moclobemide Sandoz</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Moclobemide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 16:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>76935-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Modafin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>230327</Austr>
				<PresentationName>Modafin</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
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							<Side1Marking>L233</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>230327-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Modafinil (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>276420</Austr>
				<PresentationName>APO-Modafinil</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Modafinil</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/11/2017 11:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>MOD 100</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>276420-C01-01-BL600.jpg</ImageFileName>
							</View>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Modafinil (Mylan)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>269913</Austr>
				<PresentationName>Modafinil Mylan</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Modafinil Mylan</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Modafinil (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>269914</Austr>
				<PresentationName>Modafinil Sandoz</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>27/11/2017 09:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>269914-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Modavigil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>168497</Austr>
				<PresentationName>Modavigil</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Modafinil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Modavigil</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>modafinil</ActiveIngredient>
						<ReleaseDate>2020-02-27 13:45:09.0</ReleaseDate>
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				<Images>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2020 15:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>168497-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>82350</Austr>
				<PresentationName>Modavigil</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-09-07 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Modafinil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/08/2008 10:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>m</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82350-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Moduretic</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10499</Austr>
				<PresentationName>Moduretic</PresentationName>
    			<PresentionStrength>50mg/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Amiloride hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<DateEffective>20/03/2013 11:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
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							<Shape>diamond-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10499-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Mogadon</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>13751</Austr>
				<PresentationName>Mogadon</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nitrazepam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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						<QualiferData></QualiferData>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>nitrazepam</ActiveIngredient>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>16/01/2009 13:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ICN as a sleeping face</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>13751-A01-01-BL600.jpg</ImageFileName>
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							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>13751-B01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Monace</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>101878</Austr>
				<PresentationName>Monace</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fosinopril sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Monace</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>fosinopril sodium</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>arc-rectangular</Shape>
							<Side1Marking>FS 10</Side1Marking>
							<Side2Marking>G G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101878-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>101901</Austr>
				<PresentationName>Monace</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fosinopril sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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								<Format>PDF</Format>
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						<ActiveIngredient>fosinopril sodium</ActiveIngredient>
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				<Images>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>FS 20</Side1Marking>
							<Side2Marking>G G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101901-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Monodur </brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>59600</Austr>
				<PresentationName>Monodur</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Isosorbide mononitrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Monodur</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ixcmonod10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>isosorbide mononitrate</ActiveIngredient>
						<ReleaseDate>2022-06-28 08:46:54.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 11:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>A ID</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>59600-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>64284</Austr>
				<PresentationName>Monodur</PresentationName>
    			<PresentionStrength>120mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Isosorbide mononitrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Monodur</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ixcmonod10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>isosorbide mononitrate</ActiveIngredient>
						<ReleaseDate>2022-06-28 08:46:54.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 11:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>A IF</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>64284-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Monofeme</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>215574</Austr>
				<PresentationName>Monofeme</PresentationName>
    			<PresentionStrength>150mcg/30mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Levonorgestrel,Ethinyloestradiol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Monofeme</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcmonot11219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levonorgestrel with ethinylestradiol</ActiveIngredient>
						<ReleaseDate>2019-12-12 15:07:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/05/2014 13:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>215574-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>215574-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>296399</Austr>
				<PresentationName>Monofeme</PresentationName>
    			<PresentionStrength>150mcg/30mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>ethinylestradiol,Levonorgestrel</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Monofeme</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcmonot11219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levonorgestrel with ethinylestradiol</ActiveIngredient>
						<ReleaseDate>2019-12-12 15:07:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/03/2020 12:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>296399-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>296399-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Montair</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>184827</Austr>
				<PresentationName>Montair</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 11:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink, mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>M5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184827-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>184829</Austr>
				<PresentationName>Montair</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 11:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>M4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184829-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>184836</Austr>
				<PresentationName>Montair</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 11:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rounded square</Shape>
							<Side1Marking>M 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184836-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Montelair</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>184825</Austr>
				<PresentationName>Montelair</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/03/2019 14:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>M5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184825-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>184828</Austr>
				<PresentationName>Montelair</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/03/2019 14:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rounded square</Shape>
							<Side1Marking>M 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184828-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>184837</Austr>
				<PresentationName>Montelair</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/03/2019 14:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>M4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184837-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Montelukast sodium (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>170248</Austr>
				<PresentationName>APO-Montelukast</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-10-21 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Montelukast sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rounded square</Shape>
							<Side1Marking>M10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>170248-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179115</Austr>
				<PresentationName>APO-Montelukast</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-10-21 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Montelukast sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2014 09:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>M5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179115-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179118</Austr>
				<PresentationName>APO-Montelukast</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-10-21 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Montelukast sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/09/2014 11:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>M4</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179118-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>184824</Austr>
				<PresentationName>Montelukast Apotex</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/03/2020 22:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>M5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184824-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>184831</Austr>
				<PresentationName>Montelukast Apotex</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/03/2020 22:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>M4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184831-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>184834</Austr>
				<PresentationName>Montelukast Apotex</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/03/2020 22:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rounded square</Shape>
							<Side1Marking>M 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184834-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Montelukast sodium (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>189224</Austr>
				<PresentationName>Montelukast GH</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 11:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light brown</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>189224-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>189229</Austr>
				<PresentationName>Montelukast GH</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/05/2017 15:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>189229-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>189240</Austr>
				<PresentationName>Montelukast GH</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/05/2017 15:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>189240-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Montelukast sodium (Mylan)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>323025</Austr>
				<PresentationName>Montelukast Mylan</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablet</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Montelukast Mylan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcmonte10820</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>montelukast sodium</ActiveIngredient>
						<ReleaseDate>2020-08-05 15:41:30.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/06/2021 14:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>M5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>323025-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>323026</Austr>
				<PresentationName>Montelukast Mylan</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablet</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Montelukast Mylan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcmonte10820</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>montelukast sodium</ActiveIngredient>
						<ReleaseDate>2020-08-05 15:41:30.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/06/2021 14:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>M4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>323026-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Montelukast sodium (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>184826</Austr>
				<PresentationName>Pharmacor Montelukast</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/12/2013 15:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>M5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184826-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>184835</Austr>
				<PresentationName>Pharmacor Montelukast</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/12/2013 15:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rounded square</Shape>
							<Side1Marking>M 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184835-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>184838</Austr>
				<PresentationName>Pharmacor Montelukast</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/12/2013 15:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>M4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184838-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Montelukast sodium (Sandoz)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>184830</Austr>
				<PresentationName>Montelukast Sandoz</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/09/2013 11:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rounded square</Shape>
							<Side1Marking>M 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184830-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>184832</Austr>
				<PresentationName>Montelukast Sandoz</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/09/2013 11:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>mottled pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>M4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184832-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>184833</Austr>
				<PresentationName>Montelukast Sandoz</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/09/2013 11:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>mottled pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>M5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184833-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Morphine Sulfate (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>132251</Austr>
				<PresentationName>Morphine MR Apotex</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/05/2012 11:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>buff</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>132251-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>132254</Austr>
				<PresentationName>Morphine MR Apotex</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/05/2012 11:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>violet</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>30</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>132254-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>132256</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient></TGAIngredient>
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					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
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							<Side2Marking></Side2Marking>
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							<View>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>132258</Austr>
				<PresentationName>Morphine MR Apotex</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>132258-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Morphine Sulfate (Mylan)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>225421</Austr>
				<PresentationName>Morphine MR Mylan</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Side2Marking></Side2Marking>
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							<View>
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							</Views>
						</Phase>
					</Versions>
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			</Presentations>
			<Presentations>
				<Austr>225422</Austr>
				<PresentationName>Morphine MR Mylan</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Morphine MR Mylan</DocumentName>
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						<ActiveIngredient>morphine sulfate pentahydrate</ActiveIngredient>
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						<VersionSequence>1</VersionSequence>
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						<DateEffective>26/03/2021 13:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>violet</Colour>
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							<Shape>round</Shape>
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							<Side2Marking></Side2Marking>
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							<View>
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			</Presentations>
			<Presentations>
				<Austr>225423</Austr>
				<PresentationName>Morphine MR Mylan</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Morphine MR Mylan</DocumentName>
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						<ActiveIngredient>morphine sulfate pentahydrate</ActiveIngredient>
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							<PhaseItem>1</PhaseItem>
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			</Presentations>
			<Presentations>
				<Austr>225424</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
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							<Views>
							<View>
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							</Views>
						</Phase>
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			</Presentations>
		</Brand><Brand>
			<brandname>Motilium</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>39510</Austr>
				<PresentationName>Motilium</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<Side1Marking>M 10</Side1Marking>
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							<Views>
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		</Brand><Brand>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>142228</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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							<Views>
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			<Presentations>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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							<Views>
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		</Brand><Brand>
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			<Presentations>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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			<Presentations>
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			<Presentations>
				<Austr>287646</Austr>
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			<isamtbrand>true</isamtbrand>
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								<ImageFileName>300132-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>MS Contin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>210776</Austr>
				<PresentationName>MS Contin</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Morphine sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/07/2015 11:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light tan</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>10 mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>210776-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>43086</Austr>
				<PresentationName>MS Contin</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Morphine sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/08/2010 12:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>purple</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>30 mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>43086-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>43087</Austr>
				<PresentationName>MS Contin</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Morphine sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/08/2010 12:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>60 mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>43087-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>43088</Austr>
				<PresentationName>MS Contin</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Morphine sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/08/2010 12:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>grey</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>100 mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>43088-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>51760</Austr>
				<PresentationName>MS Contin</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Morphine sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/08/2010 12:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>5 mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>51760-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>78208</Austr>
				<PresentationName>MS Contin</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Morphine sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/08/2010 12:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>15 mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>78208-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>78209</Austr>
				<PresentationName>MS Contin</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Morphine sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/08/2010 12:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>teal green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>200 mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>78209-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>MS Mono</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>74150</Austr>
				<PresentationName>MS Mono</PresentationName>
    			<PresentionStrength>120mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Morphine sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/08/2010 10:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>olive</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>MS OD</Side1Marking>
							<Side2Marking>120</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>74150-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>74152</Austr>
				<PresentationName>MS Mono</PresentationName>
    			<PresentionStrength>90mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Morphine sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/08/2010 10:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>pink</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>MS OD</Side1Marking>
							<Side2Marking>90</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>74152-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>74154</Austr>
				<PresentationName>MS Mono</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Morphine sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/08/2010 10:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>brown</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>MS OD</Side1Marking>
							<Side2Marking>60</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>74154-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>74156</Austr>
				<PresentationName>MS Mono</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Morphine sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/08/2010 10:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>MS OD</Side1Marking>
							<Side2Marking>30</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>74156-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Murelax</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>12952</Austr>
				<PresentationName>Murelax</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>30</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>12952-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Mycobutin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>55038</Austr>
				<PresentationName>Mycobutin</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rifabutin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Mycobutin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcmycoc10721</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>rifabutin</ActiveIngredient>
						<ReleaseDate>2021-07-13 14:40:23.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/09/2011 16:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque and red-brown</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>MYCOBUTIN</Side1Marking>
							<Side2Marking>Pharmacia &amp; Upjohn</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>55038-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>MycoCept</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>235571</Austr>
				<PresentationName>MycoCept</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/11/2019 15:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>purple</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>AHI</Side1Marking>
							<Side2Marking>500</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>235571-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Mycophenolate mofetil (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>164416</Austr>
				<PresentationName>Mycophenolate AN</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/03/2019 16:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>purple</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>AHI</Side1Marking>
							<Side2Marking>500</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>164416-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Mycophenolate mofetil (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>168109</Austr>
				<PresentationName>APO-Mycophenolate Capsules</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mycophenolate mofetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/07/2012 11:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque blue and opaque pink</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
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							<Side1Marking>MYC500</Side1Marking>
							<Side2Marking>APO</Side2Marking>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
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    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
							<Colour>purple</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>AHI</Side1Marking>
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								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
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				<PresentationName>Pharmacor Mycophenolate</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Capsules</DoseForm>
							<Colour>blue and brown</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>266</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Mycophenolate Mofetil (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>148225</Austr>
				<PresentationName>Mycophenolate Sandoz</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mycophenolate mofetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
							<Colour>lavendar</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>148227</Austr>
				<PresentationName>Mycophenolate Sandoz</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mycophenolate mofetil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue and orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
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							<Views>
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		</Brand><Brand>
			<brandname>Mydol</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>147714</Austr>
				<PresentationName>Mydol</PresentationName>
    			<PresentionStrength>500mg/10mg/5.1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>24/08/2009 12:56</DateEffective>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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			</Presentations>
		</Brand><Brand>
			<brandname>Mydol 15</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>188381</Austr>
				<PresentationName>Mydol 15</PresentationName>
    			<PresentionStrength>500mg/15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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						</Phase>
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			</Presentations>
		</Brand><Brand>
			<brandname>Myfortic</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>91939</Austr>
				<PresentationName>Myfortic</PresentationName>
    			<PresentionStrength>180mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mycophenolate sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<QualiferData></QualiferData>
						<DocumentName>Myfortic</DocumentName>
						<DocumentTypes>
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								<Format>PDF</Format>
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						<ActiveIngredient>mycophenolate sodium</ActiveIngredient>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
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							<Side1Marking>C</Side1Marking>
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			<Presentations>
				<Austr>91940</Austr>
				<PresentationName>Myfortic</PresentationName>
    			<PresentionStrength>360mg</PresentionStrength>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mycophenolate sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
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			<brandname>Myleran</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>68028</Austr>
				<PresentationName>Myleran</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Busulfan</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Shape>round</Shape>
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			<brandname>Mysoline</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>11231</Austr>
				<PresentationName>Mysoline</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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			<brandname>Naltrexone (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
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			<brandname>Naltrexone (Generic Health)</brandname>
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			<brandname>Napamide</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>55355</Austr>
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			<brandname>Naprogesic</brandname>
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				<Austr>75501</Austr>
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			<brandname>Naprosyn</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10173</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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							<Colour>peach</Colour>
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								<ViewLabel>C</ViewLabel>
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			<Presentations>
				<Austr>10174</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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			<Presentations>
				<Austr>65246</Austr>
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    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Naproxen</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Shape>oblong</Shape>
							<Side1Marking>NPR LE 500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>65246-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
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			<Presentations>
				<Austr>65247</Austr>
				<PresentationName>Naprosyn</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Naproxen</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Shape>round</Shape>
							<Side1Marking>NPR LE 250</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>65247-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Naproxen Sodium (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>195787</Austr>
				<PresentationName>Pharmacy Action Period Pain Relief</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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					<Versions>
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							<PhaseItem>1</PhaseItem>
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							<Side2Marking></Side2Marking>
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							<View>
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			<brandname>Naramig</brandname>
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			<Presentations>
				<Austr>62900</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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					<Versions>
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							<PhaseItem>1</PhaseItem>
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							<Shape>D-shaped</Shape>
							<Side1Marking>GX CE5</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
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			<brandname>Nardil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>93600</Austr>
				<PresentationName>Nardil</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
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			</Presentations>
		</Brand><Brand>
			<brandname>Natrilix</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>45361</Austr>
				<PresentationName>Natrilix</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
				<Austr>66849</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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							<View>
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								<ImageFileName>99558-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Nebilet</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>148873</Austr>
				<PresentationName>Nebilet</PresentationName>
    			<PresentionStrength>1.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nebivolol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Nebilet tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fkcnebit11120</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>nebivolol hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-11-25 15:37:11.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/07/2010 08:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>148873-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>148874</Austr>
				<PresentationName>Nebilet</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nebivolol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Nebilet tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fkcnebit11120</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>nebivolol hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-11-25 15:37:11.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/07/2010 08:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>148874-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>148875</Austr>
				<PresentationName>Nebilet</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nebivolol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Nebilet tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fkcnebit11120</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>nebivolol hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-11-25 15:37:11.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/07/2010 08:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>148875-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Nebivolol (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>281795</Austr>
				<PresentationName>APO-Nebivolol</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nebivolol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/09/2018 09:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>APO N5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>281795-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>281798</Austr>
				<PresentationName>APO-Nebivolol</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nebivolol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/09/2018 09:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>N10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>281798-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>281799</Austr>
				<PresentationName>APO-Nebivolol</PresentationName>
    			<PresentionStrength>1.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nebivolol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/09/2018 09:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>APO 1.25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>281799-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Neo-Mercazole</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>194296</Austr>
				<PresentationName>Neo-Mercazole</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Carbimazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Neo-Mercazole</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ghcneome10921</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>carbimazole</ActiveIngredient>
						<ReleaseDate>2021-09-13 14:02:53.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/08/2013 11:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>Neo 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>194296-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Neoral</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>49722</Austr>
				<PresentationName>Neoral</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Cyclosporin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Neoral</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcneoor11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ciclosporin</ActiveIngredient>
						<ReleaseDate>2022-10-25 11:21:11.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2010 13:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue-grey</Colour>
							<Scoring></Scoring>
							<Shape>oval</Shape>
							<Side1Marking>NVR 25 mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>49722-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>49723</Austr>
				<PresentationName>Neoral</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Cyclosporin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Neoral</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcneoor11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ciclosporin</ActiveIngredient>
						<ReleaseDate>2022-10-25 11:21:11.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2010 13:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow-white</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>NVR 50mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>49723-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>49724</Austr>
				<PresentationName>Neoral</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Cyclosporin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Neoral</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcneoor11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ciclosporin</ActiveIngredient>
						<ReleaseDate>2022-10-25 11:21:11.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/01/2011 13:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue-grey</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>NVR 100mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>49724-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>59614</Austr>
				<PresentationName>Neoral</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Cyclosporin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Neoral</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcneoor11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ciclosporin</ActiveIngredient>
						<ReleaseDate>2022-10-25 11:21:11.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/01/2011 13:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow-white</Colour>
							<Scoring></Scoring>
							<Shape>oval</Shape>
							<Side1Marking>NVR 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>59614-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Neosulf</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>17707</Austr>
				<PresentationName>Neosulf</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Neomycin sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>17707-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>17707-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Neotigason</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>52455</Austr>
				<PresentationName>Neotigason</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Acitretin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Neotigason</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcneoti10718</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>acitretin</ActiveIngredient>
						<ReleaseDate>2018-08-01 11:47:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/11/2018 16:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>brown opaque and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>52455-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>52456</Austr>
				<PresentationName>Neotigason</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Acitretin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Neotigason</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcneoti10718</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>acitretin</ActiveIngredient>
						<ReleaseDate>2018-08-01 11:47:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/11/2018 16:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>brown opaque and yellow opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>52456-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Nesina</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>199539</Austr>
				<PresentationName>Nesina</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>alogliptin benzoate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Nesina</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tkcnesin10921</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>alogliptin benzoate</ActiveIngredient>
						<ReleaseDate>2021-09-20 14:05:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/11/2014 13:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>TAK ALG-25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199539-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199541</Austr>
				<PresentationName>Nesina</PresentationName>
    			<PresentionStrength>6.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>alogliptin benzoate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Nesina</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tkcnesin10921</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>alogliptin benzoate</ActiveIngredient>
						<ReleaseDate>2021-09-20 14:05:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/11/2014 13:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>TAK ALG-6.25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199541-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199543</Austr>
				<PresentationName>Nesina</PresentationName>
    			<PresentionStrength>12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>alogliptin benzoate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Nesina</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tkcnesin10921</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>alogliptin benzoate</ActiveIngredient>
						<ReleaseDate>2021-09-20 14:05:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/11/2014 13:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>TAK ALG-12.5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199543-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Nesina Met</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>202306</Austr>
				<PresentationName>Nesina Met</PresentationName>
    			<PresentionStrength>12.5mg/850mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>metformin hydrochloride,alogliptin benzoate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Nesina Met</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tkcnesmt10921</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>alogliptin benzoate with metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-09-20 14:05:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/11/2014 13:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>322M</Side1Marking>
							<Side2Marking>12.5/850</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>202306-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>202308</Austr>
				<PresentationName>Nesina Met</PresentationName>
    			<PresentionStrength>12.5mg/500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>alogliptin benzoate,metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Nesina Met</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tkcnesmt10921</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>alogliptin benzoate with metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-09-20 14:05:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/11/2014 13:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>322M</Side1Marking>
							<Side2Marking>12.5/500</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>202308-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>202309</Austr>
				<PresentationName>Nesina Met</PresentationName>
    			<PresentionStrength>12.5mg/1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>metformin hydrochloride,alogliptin benzoate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Nesina Met</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tkcnesmt10921</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>alogliptin benzoate with metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-09-20 14:05:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/11/2014 13:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>322M</Side1Marking>
							<Side2Marking>12.5/1000</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>202309-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Neulactil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>27523</Austr>
				<PresentationName>Neulactil</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pericyazine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Neulactil</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcneula10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>periciazine</ActiveIngredient>
						<ReleaseDate>2022-09-13 08:30:54.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>27523-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>27524</Austr>
				<PresentationName>Neulactil</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pericyazine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Neulactil</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcneula10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>periciazine</ActiveIngredient>
						<ReleaseDate>2022-09-13 08:30:54.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NEULACTIL</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>27524-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Neupro</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>131370</Austr>
				<PresentationName>Neupro</PresentationName>
    			<PresentionStrength>2mg/24h</PresentionStrength>
    			<PresentationForm>Patches</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>sachet</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/01/2009 13:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Patches</DoseForm>
							<Colour>tan</Colour>
							<Scoring></Scoring>
							<Shape>square-shaped with rounded edges</Shape>
							<Side1Marking>Neupro 2mg/24h</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>131370-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel></ViewLabel>
    							<ImageFileName>NO IMAGE</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>131381</Austr>
				<PresentationName>Neupro</PresentationName>
    			<PresentionStrength>4mg/24h</PresentionStrength>
    			<PresentationForm>Patches</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>sachet</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/01/2009 13:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Patches</DoseForm>
							<Colour>tan</Colour>
							<Scoring></Scoring>
							<Shape>square-shaped with rounded edges</Shape>
							<Side1Marking>Neupro 4mg/24h</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>131381-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel></ViewLabel>
    							<ImageFileName>NO IMAGE</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>131382</Austr>
				<PresentationName>Neupro</PresentationName>
    			<PresentionStrength>6mg/24h</PresentionStrength>
    			<PresentationForm>Patches</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>sachet</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/01/2009 13:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Patches</DoseForm>
							<Colour>tan</Colour>
							<Scoring></Scoring>
							<Shape>square-shaped with rounded edges</Shape>
							<Side1Marking>Neupro 6mg/24h</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>131382-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel></ViewLabel>
    							<ImageFileName>NO IMAGE</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>131383</Austr>
				<PresentationName>Neupro</PresentationName>
    			<PresentionStrength>8mg/24h</PresentionStrength>
    			<PresentationForm>Patches</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>sachet</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/01/2009 13:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Patches</DoseForm>
							<Colour>tan</Colour>
							<Scoring></Scoring>
							<Shape>square-shaped with rounded edges</Shape>
							<Side1Marking>Neupro 8mg/24h</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>131383-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel></ViewLabel>
    							<ImageFileName>NO IMAGE</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Neurontin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>66005</Austr>
				<PresentationName>Neurontin</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Neurontin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocneuro11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>gabapentin</ActiveIngredient>
						<ReleaseDate>2022-11-10 10:11:19.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/09/2008 11:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Neurontin 400 mg</Side1Marking>
							<Side2Marking>PD</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>66005-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>66008</Austr>
				<PresentationName>Neurontin</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Neurontin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocneuro11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>gabapentin</ActiveIngredient>
						<ReleaseDate>2022-11-10 10:11:19.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/09/2008 11:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Neurontin 300 mg</Side1Marking>
							<Side2Marking>PD</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>66008-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>71791</Austr>
				<PresentationName>Neurontin</PresentationName>
    			<PresentionStrength>800mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Neurontin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocneuro11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>gabapentin</ActiveIngredient>
						<ReleaseDate>2022-11-10 10:11:19.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/06/2011 10:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>NT 26</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>71791-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>71793</Austr>
				<PresentationName>Neurontin</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Neurontin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocneuro11022</Filename>
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						</DocumentTypes>
						<ActiveIngredient>gabapentin</ActiveIngredient>
						<ReleaseDate>2022-11-10 10:11:19.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/09/2011 16:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>NT 16</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>71793-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>74067</Austr>
				<PresentationName>Neurontin</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Neurontin</DocumentName>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>gabapentin</ActiveIngredient>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/09/2008 11:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Neurontin 100 mg</Side1Marking>
							<Side2Marking>PD</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>74067-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Nevirapine (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>272979</Austr>
				<PresentationName>Nevirapine XR APOTEX</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-10-21 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nevirapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/11/2017 11:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>NV400</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>272979-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Nevirapine (Viatris)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>167307</Austr>
				<PresentationName>Nevirapine Viatris</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Nevirapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Nevirapine Viatris</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcnevir10922</Filename>
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						</DocumentTypes>
						<ActiveIngredient>nevirapine</ActiveIngredient>
						<ReleaseDate>2022-09-30 13:24:30.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>NE 200</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167307-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Nexavar</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>123158</Austr>
				<PresentationName>Nexavar</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/04/2010 11:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>200</Side1Marking>
							<Side2Marking>BAYER Cross</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>123158-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Nexazole</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>205824</Austr>
				<PresentationName>Nexazole</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>CE</Side1Marking>
							<Side2Marking>40</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>205824-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>205846</Austr>
				<PresentationName>Nexazole</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>10/07/2018 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>CE</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>205846-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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			</Presentations>
		</Brand><Brand>
			<brandname>Nexium</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>74133</Austr>
				<PresentationName>Nexium</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Esomeprazole magnesium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR>97190</IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Nexium</DocumentName>
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						<ActiveIngredient>esomeprazole magnesium trihydrate</ActiveIngredient>
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				<Images>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/09/2008 14:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
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							<Colour>light pink</Colour>
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							<Shape>oblong</Shape>
							<Side1Marking>A EH</Side1Marking>
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							<Views>
							<View>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>74134</Austr>
				<PresentationName>Nexium</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Esomeprazole magnesium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Nexium</DocumentName>
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						<DateEffective>15/09/2008 14:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>A EI</Side1Marking>
							<Side2Marking>40 MG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>74134-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>97190</Austr>
				<PresentationName>Nexium HP7 </PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Combination Pack</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>composite pack</Container>
    			<TGAIngredient>Clarithromycin,Amoxycillin,Esomeprazole magnesium trihydrate</TGAIngredient>
    			<IsAMasterPack>Yes</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/07/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>None</DoseForm>
							<Colour></Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
								<View></View>
								<ImageFileName />
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Niaspan</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>106929</Austr>
				<PresentationName>Niaspan</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/06/2009 13:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>106929-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>106931</Austr>
				<PresentationName>Niaspan</PresentationName>
    			<PresentionStrength>750mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/06/2009 13:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>750</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>106931-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>106934</Austr>
				<PresentationName>Niaspan</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/06/2009 13:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>106934-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Nicabate</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>81977</Austr>
				<PresentationName>Nicabate</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/03/2009 16:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Lozenges</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NL 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>81977-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>81977-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>81978</Austr>
				<PresentationName>Nicabate</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/03/2009 16:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Lozenges</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NL 4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>81978-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>81978-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Nicotinic Acid</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>27193</Austr>
				<PresentationName>Nicotinic Acid</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Nicotinic Acid</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcnicac11019</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>nicotinic acid</ActiveIngredient>
						<ReleaseDate>2019-10-10 16:25:03.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>27193-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Nidem</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>79023</Austr>
				<PresentationName>Nidem</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>79023-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Nifedipine (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>152207</Austr>
				<PresentationName>Apo-Nifedipine XR</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/03/2010 13:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>30</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152207-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>152208</Austr>
				<PresentationName>Apo-Nifedipine XR</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/03/2010 13:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>60</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152208-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Nimotop</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>43100</Austr>
				<PresentationName>Nimotop</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/04/2010 11:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SK</Side1Marking>
							<Side2Marking>Bayer Cross</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>43100-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Nitrofurantoin (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>299383</Austr>
				<PresentationName>APO-Nitrofurantoin</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>nitrofurantoin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2022 11:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow opaque and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>299383-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Nizac</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>96961</Austr>
				<PresentationName>Nizac</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nizatidine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/11/2008 13:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light yellow and dark yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>N150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96961-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>96963</Austr>
				<PresentationName>Nizac</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nizatidine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/11/2008 13:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light yellow and brown</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>N300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96963-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Nolvadex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>11232</Austr>
				<PresentationName>Nolvadex &amp; Nolvadex D</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tamoxifen citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Nolvadex</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apcnolva10921</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tamoxifen citrate</ActiveIngredient>
						<ReleaseDate>2021-09-13 11:37:06.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 10:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>eight-sided</Shape>
							<Side1Marking>NOLVADEX D</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>11232-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>11233</Austr>
				<PresentationName>Nolvadex &amp; Nolvadex D</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tamoxifen citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Nolvadex</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apcnolva10921</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tamoxifen citrate</ActiveIngredient>
						<ReleaseDate>2021-09-13 11:37:06.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 11:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NOLVADEX 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>11233-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Nordette</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>215575</Austr>
				<PresentationName>Nordette</PresentationName>
    			<PresentionStrength>150mcg/30mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ethinyloestradiol,Levonorgestrel</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Nordette</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcnordt11219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levonorgestrel with ethinylestradiol</ActiveIngredient>
						<ReleaseDate>2019-12-12 14:41:16.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/05/2014 13:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>215575-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>215575-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>296400</Austr>
				<PresentationName>Nordette</PresentationName>
    			<PresentionStrength>150mcg/30mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>ethinylestradiol,Levonorgestrel</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Nordette</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcnordt11219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levonorgestrel with ethinylestradiol</ActiveIngredient>
						<ReleaseDate>2019-12-12 14:41:16.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/03/2020 12:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>296400-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>296400-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Nordip</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>133146</Austr>
				<PresentationName>Nordip</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Nordip</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcnordi10819</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amlodipine besilate</ActiveIngredient>
						<ReleaseDate>2019-08-22 08:19:10.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/10/2010 16:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AB 10</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133146-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>133159</Austr>
				<PresentationName>Nordip</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Nordip</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcnordi10819</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amlodipine besilate</ActiveIngredient>
						<ReleaseDate>2019-08-22 08:19:10.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/10/2010 16:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AB 5</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133159-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Norflex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10573</Austr>
				<PresentationName>Norflex</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Orphenadrine citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/03/2012 14:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>N X</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10573-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Norfloxacin (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>155546</Austr>
				<PresentationName>APO-Norfloxacin</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>13/07/2010 12:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>N F</Side1Marking>
							<Side2Marking>Arrow logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>155546-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Norfloxacin (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>79112</Austr>
				<PresentationName>Norfloxacin-GA</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 11:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>CD</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>79112-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Norgesic</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10574</Austr>
				<PresentationName>Norgesic</PresentationName>
    			<PresentionStrength>35mg/450mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>jar</Container>
    			<TGAIngredient>Orphenadrine citrate,Paracetamol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/12/2010 11:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>N/C</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>10574-A01-02-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>10574-B01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Noriday</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10052</Austr>
				<PresentationName>Noriday 28-Day</PresentationName>
    			<PresentionStrength>350mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Norethisterone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Noriday</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcnorit10220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>norethisterone</ActiveIngredient>
						<ReleaseDate>2020-03-16 15:24:09.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/09/2011 16:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NY</Side1Marking>
							<Side2Marking>SEARLE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10052-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Norimin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>62133</Austr>
				<PresentationName>Norimin 28 day</PresentationName>
    			<PresentionStrength>500mcg/35mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ethinyloestradiol,Norethisterone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Norimin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcnormt10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>norethisterone with ethinylestradiol</ActiveIngredient>
						<ReleaseDate>2022-06-17 09:22:14.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/09/2008 11:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>BX</Side1Marking>
							<Side2Marking>SEARLE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62133-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>P</Side1Marking>
							<Side2Marking>SEARLE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62133-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>62136</Austr>
				<PresentationName>Norimin-1 28 day</PresentationName>
    			<PresentionStrength>1mg/35mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ethinyloestradiol,Norethisterone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Norimin-1</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcnor1t10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>norethisterone with ethinylestradiol</ActiveIngredient>
						<ReleaseDate>2022-06-17 09:32:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/09/2011 16:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>BX</Side1Marking>
							<Side2Marking>SEARLE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62136-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>P</Side1Marking>
							<Side2Marking>SEARLE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62136-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Norinyl</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>61643</Austr>
				<PresentationName>Norinyl-1 28 Day</PresentationName>
    			<PresentionStrength>1mg/50mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mestranol,Norethisterone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Norinyl-1</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcnoryt10220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>norethisterone with mestranol</ActiveIngredient>
						<ReleaseDate>2020-03-16 15:24:14.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/09/2011 10:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>1</Side1Marking>
							<Side2Marking>SEARLE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>61643-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>P</Side1Marking>
							<Side2Marking>SEARLE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>61643-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>61648</Austr>
				<PresentationName>Norinyl-1 21 Day</PresentationName>
    			<PresentionStrength>1mg/50mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mestranol,Norethisterone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/09/2008 11:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>1</Side1Marking>
							<Side2Marking>SEARLE</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>61648-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Norlevo</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>166340</Austr>
				<PresentationName>Norlevo-1</PresentationName>
    			<PresentionStrength>1.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NL 1.5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166340-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Normison</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>41637</Austr>
				<PresentationName>Normison</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>S</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>41637-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Norprolac</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>48991</Austr>
				<PresentationName>Norprolac</PresentationName>
    			<PresentionStrength>75mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quinagolide hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Norprolac</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fpcnorpt11019</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>quinagolide hydrochloride</ActiveIngredient>
						<ReleaseDate>2019-10-23 13:51:19.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>17/09/2008 14:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NORPROLAC</Side1Marking>
							<Side2Marking>75</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>48991-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>48993</Austr>
				<PresentationName>Norprolac</PresentationName>
    			<PresentionStrength>25mcg/50mcg</PresentionStrength>
    			<PresentationForm>Starter Pack</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quinagolide hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Norprolac</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fpcnorpt11019</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>quinagolide hydrochloride</ActiveIngredient>
						<ReleaseDate>2019-10-23 13:51:19.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/09/2008 14:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NORPROLAC</Side1Marking>
							<Side2Marking>25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>48993-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NORPROLAC</Side1Marking>
							<Side2Marking>50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>48993-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>NortriTABS</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>220997</Austr>
				<PresentationName>NortriTABS</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nortriptyline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>NortriTABS</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ghcnortr11116</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>nortriptyline hydrochloride</ActiveIngredient>
						<ReleaseDate>2017-06-27 13:38:02.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/10/2017 10:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NM</Side1Marking>
							<Side2Marking>25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>220997-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>220998</Austr>
				<PresentationName>NortriTABS</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nortriptyline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>NortriTABS</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ghcnortr11116</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>nortriptyline hydrochloride</ActiveIngredient>
						<ReleaseDate>2017-06-27 13:38:02.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/10/2017 10:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NM</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>220998-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Norvasc</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>42902</Austr>
				<PresentationName>Norvasc</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/09/2018 14:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>emerald-shaped</Shape>
							<Side1Marking>AML 5</Side1Marking>
							<Side2Marking>Pfizer</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>42902-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>42903</Austr>
				<PresentationName>Norvasc</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/09/2018 14:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>emerald-shaped</Shape>
							<Side1Marking>AML-10</Side1Marking>
							<Side2Marking>Pfizer</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>42903-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Norvir</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>158301</Austr>
				<PresentationName>Norvir</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Ritonavir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Norvir</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>vecnorvt20820</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ritonavir</ActiveIngredient>
						<ReleaseDate>2020-08-24 14:38:46.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/12/2011 10:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>ovaloid</Shape>
							<Side1Marking>Abbott logo NK</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158301-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Noten</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>46250</Austr>
				<PresentationName>Noten</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atenolol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Noten</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcnoten10621</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>atenolol</ActiveIngredient>
						<ReleaseDate>2021-06-22 13:45:46.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>AT 50</Side1Marking>
							<Side2Marking>&#945;</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>46250-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>46251</Austr>
				<PresentationName>Noten</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
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			</Presentations>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<brandname>Noxicid</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>246914</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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		</Brand><Brand>
			<brandname>Nuelin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>46069</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Theophylline</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			</Presentations>
			<Presentations>
				<Austr>59526</Austr>
				<PresentationName>Nuelin SR</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Theophylline</TGAIngredient>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>59526-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>59527</Austr>
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    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Theophylline</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Shape>round</Shape>
							<Side1Marking>N L</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>59527-C01-01-BL600.jpg</ImageFileName>
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			<brandname>Nufloxib</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>149416</Austr>
				<PresentationName>Nufloxib</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-03-02 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Norfloxacin</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateEffective>06/07/2009 11:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>149416-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Nupentin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>101694</Austr>
				<PresentationName>Nupentin</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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						<ReleaseDate>2022-10-21 15:06:34.0</ReleaseDate>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>G</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101694-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101696</Austr>
				<PresentationName>Nupentin</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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			<Presentations>
				<Austr>101698</Austr>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
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						<DateEffective>05/06/2012 13:48</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Colour>white to off-white</Colour>
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							<Shape>oval</Shape>
							<Side1Marking>G 25</Side1Marking>
							<Side2Marking>MYLAN</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>174062-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>174063</Austr>
				<PresentationName>Nupentin Tabs</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Gabapentin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/06/2012 13:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>G 24</Side1Marking>
							<Side2Marking>MYLAN</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>174063-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Nurofen</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>116620</Austr>
				<PresentationName>Nurofen Plus</PresentationName>
    			<PresentionStrength>12.8mg/200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ibuprofen,codeine phosphate hemihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/03/2011 10:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>N+</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>116620-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>120354</Austr>
				<PresentationName>Nurofen Tension Headache</PresentationName>
    			<PresentionStrength>342mg</PresentionStrength>
    			<PresentationForm>Caplets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/05/2011 11:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Caplets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>NMP</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>120354-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127272</Austr>
				<PresentationName>Nurofen</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/03/2011 10:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NUROFEN</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127272-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127273</Austr>
				<PresentationName>Nurofen</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/03/2011 10:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NUROFEN</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127273-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127287</Austr>
				<PresentationName>Nurofen Caplets</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Caplets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/03/2011 10:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Caplets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>NUROFEN</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127287-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>134618</Austr>
				<PresentationName>Nurofen Period Pain</PresentationName>
    			<PresentionStrength>342mg</PresentionStrength>
    			<PresentationForm>Caplets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/03/2011 10:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Caplets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>NMP</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>134618-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>141995</Austr>
				<PresentationName>Nurofen 400 Double Strength</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/02/2011 13:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Liquid Capsules</DoseForm>
							<Colour>red</Colour>
							<Scoring></Scoring>
							<Shape>oval</Shape>
							<Side1Marking>N400</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>141995-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>141996</Austr>
				<PresentationName>Nurofen 400 Double Strength</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/02/2011 13:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NUROFEN 400</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>141996-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>141996-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>142080</Austr>
				<PresentationName>Nurofen Back Pain</PresentationName>
    			<PresentionStrength>342mg</PresentionStrength>
    			<PresentationForm>Caplets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/05/2011 11:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Caplets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>NMP</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>142080-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>65640</Austr>
				<PresentationName>Nurofen Cold and Flu</PresentationName>
    			<PresentionStrength>200mg/30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/01/2012 15:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CN Logo</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>65640-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>95381</Austr>
				<PresentationName>Nurofen</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/03/2011 10:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NUROFEN</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>95381-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>96115</Austr>
				<PresentationName>Nurofen Liquid Capsules</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<DateEffective>11/03/2011 10:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>NUROFEN</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96115-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>96215</Austr>
				<PresentationName>Nurofen Migraine Pain</PresentationName>
    			<PresentionStrength>342mg</PresentionStrength>
    			<PresentationForm>Caplets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/03/2011 10:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Caplets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>NMP</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96215-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Nuromol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>225322</Austr>
				<PresentationName>Nuromol</PresentationName>
    			<PresentionStrength>200mg/500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/10/2019 11:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white pearlescent</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>helix </Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>225322-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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			</Presentations>
		</Brand><Brand>
			<brandname>Nuvigil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>226558</Austr>
				<PresentationName>Nuvigil</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>armodafinil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Nuvigil (TB)</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>armodafinil</ActiveIngredient>
						<ReleaseDate>2020-02-26 15:59:08.0</ReleaseDate>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2020 15:58</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
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							<Side1Marking>225</Side1Marking>
							<Side2Marking>C logo</Side2Marking>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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							<Side1Marking>205</Side1Marking>
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			<brandname>Odaplix SR</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>139608</Austr>
				<PresentationName>Odaplix SR</PresentationName>
    			<PresentionStrength>1.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<ActiveIngredient>indapamide hemihydrate</ActiveIngredient>
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						<DateEffective>26/10/2016 14:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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		</Brand><Brand>
			<brandname>Ofev</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>226065</Austr>
				<PresentationName>Ofev</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>nintedanib esilate</TGAIngredient>
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						<DateEffective>12/09/2016 14:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>peach opaque</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>Boehringer Ingelheim logo 100</Side1Marking>
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			<Presentations>
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				<PresentationName>Ofev</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>nintedanib esilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>12/09/2016 14:25</DateEffective>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
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							<Colour>brown opaque</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>Boehringer Ingelheim logo 150</Side1Marking>
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		</Brand><Brand>
			<brandname>Olanzapine (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>178992</Austr>
				<PresentationName>Olanzapine AN</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Side2Marking></Side2Marking>
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			<Presentations>
				<Austr>178993</Austr>
				<PresentationName>Olanzapine AN</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>14/09/2017 09:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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			<Presentations>
				<Austr>178998</Austr>
				<PresentationName>Olanzapine AN</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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			<Presentations>
				<Austr>179000</Austr>
				<PresentationName>Olanzapine AN</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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			</Presentations>
			<Presentations>
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				<PresentationName>Olanzapine AN ODT</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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			<Presentations>
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			<Presentations>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/07/2012 13:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>OLA 2.5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158979-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158981</Austr>
				<PresentationName>APO-Olanzapine</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-10-21 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/07/2012 13:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>OLA 5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158981-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158986</Austr>
				<PresentationName>APO-Olanzapine ODT</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/11/2017 11:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>OL 20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158986-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158987</Austr>
				<PresentationName>APO-Olanzapine</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-10-21 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>OLA 7.5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158987-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158992</Austr>
				<PresentationName>APO-Olanzapine ODT</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/11/2017 11:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>OL 15</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158992-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158995</Austr>
				<PresentationName>APO-Olanzapine ODT</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/07/2012 13:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>OL 5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158995-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>159001</Austr>
				<PresentationName>APO-Olanzapine ODT</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/11/2017 11:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>OL 10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159001-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>303714</Austr>
				<PresentationName>Olanzapine Apotex</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2022 10:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow to yellow, slightly mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>O4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>303714-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>303715</Austr>
				<PresentationName>Olanzapine Apotex</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2022 10:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow to yellow, slightly mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>O5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>303715-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>303716</Austr>
				<PresentationName>Olanzapine Apotex</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2022 10:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow to yellow, slightly mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>O6</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>303716-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>303717</Austr>
				<PresentationName>Olanzapine Apotex</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2022 10:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow to yellow, slightly mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>O7</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>303717-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olanzapine (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>178969</Austr>
				<PresentationName>Olanzapine-GA</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/06/2012 08:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>178969-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>178971</Austr>
				<PresentationName>Olanzapine-GA</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/06/2012 08:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>178971-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>178990</Austr>
				<PresentationName>Olanzapine-GA</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/06/2012 08:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>178990-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179003</Austr>
				<PresentationName>Olanzapine-GA</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/06/2012 08:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179003-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179090</Austr>
				<PresentationName>Olanzapine-GA ODT</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/06/2012 08:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179090-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179091</Austr>
				<PresentationName>Olanzapine-GA ODT</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/06/2012 08:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179091-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olanzapine (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>152124</Austr>
				<PresentationName>Olanzapine generichealth</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/04/2015 16:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>OPN 2.5</Side1Marking>
							<Side2Marking>bza</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152124-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>152167</Austr>
				<PresentationName>Olanzapine generichealth</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2015 16:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>OPN 5</Side1Marking>
							<Side2Marking>bza</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152167-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>152168</Austr>
				<PresentationName>Olanzapine generichealth</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>OPN 7.5</Side1Marking>
							<Side2Marking>bza</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152168-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>152169</Austr>
				<PresentationName>Olanzapine generichealth</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>OPN 10</Side1Marking>
							<Side2Marking>bza</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152169-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>177790</Austr>
				<PresentationName>Olanzapine ODT generichealth</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>177790-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>177793</Austr>
				<PresentationName>Olanzapine ODT generichealth</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>177793-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olanzapine (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>177119</Austr>
				<PresentationName>Pharmacor Olanzapine</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/01/2013 11:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>O3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>177119-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>177121</Austr>
				<PresentationName>Pharmacor Olanzapine</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/01/2013 11:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>O1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>177121-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>177125</Austr>
				<PresentationName>Pharmacor Olanzapine</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/01/2013 11:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>O2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>177125-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>177128</Austr>
				<PresentationName>Pharmacor Olanzapine</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/01/2013 11:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>O</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>177128-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olanzapine (Ranbaxy)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>157853</Austr>
				<PresentationName>Olanzapine RBX</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow to yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>O5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157853-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>157856</Austr>
				<PresentationName>Olanzapine RBX</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow to yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>O4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157856-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>157859</Austr>
				<PresentationName>Olanzapine RBX</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow to yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>O7</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157859-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>157860</Austr>
				<PresentationName>Olanzapine RBX</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow to yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>O6</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157860-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olanzapine (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>148450</Austr>
				<PresentationName>Olanzapine Sandoz</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 12:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>148450-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>148451</Austr>
				<PresentationName>Olanzapine Sandoz</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 12:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>148451-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>148469</Austr>
				<PresentationName>Olanzapine Sandoz</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 12:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>148469-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>148474</Austr>
				<PresentationName>Olanzapine Sandoz</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 12:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>148474-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>177800</Austr>
				<PresentationName>Olanzapine Sandoz ODT</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>177800-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>177801</Austr>
				<PresentationName>Olanzapine Sandoz ODT</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>177801-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179073</Austr>
				<PresentationName>Olanzapine Sandoz ODT (new Formulation)</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179073-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179086</Austr>
				<PresentationName>Olanzapine Sandoz ODT (new Formulation)</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179086-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179092</Austr>
				<PresentationName>Olanzapine Sandoz ODT (new Formulation)</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179092-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179093</Austr>
				<PresentationName>Olanzapine Sandoz ODT (new Formulation)</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179093-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olmekar</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>290077</Austr>
				<PresentationName>Olmekar</PresentationName>
    			<PresentionStrength>20mg/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/11/2019 15:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L75</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>290077-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>290078</Austr>
				<PresentationName>Olmekar</PresentationName>
    			<PresentionStrength>40mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/11/2019 15:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brownish red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L78</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>290078-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>290090</Austr>
				<PresentationName>Olmekar</PresentationName>
    			<PresentionStrength>40mg/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/11/2019 15:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L77</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>290090-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olmertan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>221050</Austr>
				<PresentationName>Olmertan</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L324</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>221050-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>221051</Austr>
				<PresentationName>Olmertan</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L</Side1Marking>
							<Side2Marking>323</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>221051-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olmertan Combi</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>221128</Austr>
				<PresentationName>Olmertan Combi</PresentationName>
    			<PresentionStrength>40mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L347</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>221128-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>221131</Austr>
				<PresentationName>Olmertan Combi</PresentationName>
    			<PresentionStrength>40mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L348</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>221131-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>221132</Austr>
				<PresentationName>Olmertan Combi</PresentationName>
    			<PresentionStrength>20mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L</Side1Marking>
							<Side2Marking>346</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>221132-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olmesartan medoxomil (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>221052</Austr>
				<PresentationName>APO-Olmesartan</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olmesartan medoxomil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/07/2017 15:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L</Side1Marking>
							<Side2Marking>323</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>221052-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>221063</Austr>
				<PresentationName>APO-Olmesartan</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olmesartan medoxomil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/07/2017 15:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L324</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>221063-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olmesartan medoxomil (Organon)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>273571</Austr>
				<PresentationName>Olmesartan - MYL</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olmesartan medoxomil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Olmesartan - MYL</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>olmesartan medoxomil</ActiveIngredient>
						<ReleaseDate>2022-08-17 17:33:14.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 15:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>C14</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>273571-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>273572</Austr>
				<PresentationName>Olmesartan - MYL</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olmesartan medoxomil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Olmesartan - MYL</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcolmyl10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>olmesartan medoxomil</ActiveIngredient>
						<ReleaseDate>2022-08-17 17:33:14.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 15:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C15</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>273572-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olmesartan medoxomil (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>235832</Austr>
				<PresentationName>Pharmacor Olmesartan</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/09/2017 16:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>OLM</Side1Marking>
							<Side2Marking>40</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>235832-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>235833</Austr>
				<PresentationName>Pharmacor Olmesartan</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/09/2017 16:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>OLM</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>235833-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olmesartan medoxomil (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>221056</Austr>
				<PresentationName>Olmesartan Sandoz</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olmesartan medoxomil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L324</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>221056-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>221058</Austr>
				<PresentationName>Olmesartan Sandoz</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olmesartan medoxomil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L</Side1Marking>
							<Side2Marking>323</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>221058-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olmesartan medoxomil with amlodipine besilate (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>290088</Austr>
				<PresentationName>Olmesartan/Amlodipine Apotex</PresentationName>
    			<PresentionStrength>40mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/03/2020 22:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brownish red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L78</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>290088-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>290089</Austr>
				<PresentationName>Olmesartan/Amlodipine Apotex</PresentationName>
    			<PresentionStrength>20mg/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/03/2020 22:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L75</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>290089-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>290094</Austr>
				<PresentationName>Olmesartan/Amlodipine Apotex</PresentationName>
    			<PresentionStrength>40mg/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/03/2020 22:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L77</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>290094-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olmesartan medoxomil with amlodipine besilate (Organon)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>273618</Austr>
				<PresentationName>Olmesartan/Amlodipine-MYL</PresentationName>
    			<PresentionStrength>20mg/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>amlodipine besilate,Olmesartan medoxomil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Olmesartan/Amlodipine-MYL</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcolamm10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>olmesartan medoxomil with amlodipine besilate</ActiveIngredient>
						<ReleaseDate>2022-08-17 17:34:13.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 15:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C73</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>273618-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>273619</Austr>
				<PresentationName>Olmesartan/Amlodipine-MYL</PresentationName>
    			<PresentionStrength>40mg/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olmesartan medoxomil,amlodipine besilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Olmesartan/Amlodipine-MYL</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcolamm10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>olmesartan medoxomil with amlodipine besilate</ActiveIngredient>
						<ReleaseDate>2022-08-17 17:34:13.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 15:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>cream</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C75</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>273619-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>273620</Austr>
				<PresentationName>Olmesartan/Amlodipine-MYL</PresentationName>
    			<PresentionStrength>40mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>amlodipine besilate,Olmesartan medoxomil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Olmesartan/Amlodipine-MYL</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcolamm10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>olmesartan medoxomil with amlodipine besilate</ActiveIngredient>
						<ReleaseDate>2022-08-17 17:34:13.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 15:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brownish red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C77</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>273620-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olmesartan medoxomil with amlodipine besilate and hydrochlorothiazide (Organon)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>273592</Austr>
				<PresentationName>Olmesartan/Amlodipine HCT-MYL</PresentationName>
    			<PresentionStrength>20mg/5mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>olmesartan medoxomil,hydrochlorothiazide,amlodipine besilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/06/2019 16:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C51</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>273592-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>273593</Austr>
				<PresentationName>Olmesartan/Amlodipine HCT-MYL</PresentationName>
    			<PresentionStrength>40mg/5mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>olmesartan medoxomil,hydrochlorothiazide,amlodipine besilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/06/2019 16:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C53</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>273593-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>273594</Austr>
				<PresentationName>Olmesartan/Amlodipine HCT-MYL</PresentationName>
    			<PresentionStrength>40mg/5mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>amlodipine besilate,olmesartan medoxomil,hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/06/2019 16:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C54</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>273594-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>273595</Austr>
				<PresentationName>Olmesartan/Amlodipine HCT-MYL</PresentationName>
    			<PresentionStrength>40mg/10mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>olmesartan medoxomil,hydrochlorothiazide,amlodipine besilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/06/2019 16:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>greyish red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C55</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>273595-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>273596</Austr>
				<PresentationName>Olmesartan/Amlodipine HCT-MYL</PresentationName>
    			<PresentionStrength>40mg/10mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>amlodipine besilate,hydrochlorothiazide,olmesartan medoxomil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/06/2019 16:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>greyish red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C57</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>273596-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olmesartan medoxomil with hydrochlorothiazide (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>221120</Austr>
				<PresentationName>Olmesartan HCT AN</PresentationName>
    			<PresentionStrength>40mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/03/2019 14:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L347</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>221120-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olmesartan medoxomil with hydrochlorothiazide (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>221116</Austr>
				<PresentationName>APO-Olmesartan HCTZ</PresentationName>
    			<PresentionStrength>20mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Olmesartan medoxomil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/07/2017 15:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L</Side1Marking>
							<Side2Marking>346</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>221116-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>221118</Austr>
				<PresentationName>APO-Olmesartan HCTZ</PresentationName>
    			<PresentionStrength>40mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olmesartan medoxomil,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/07/2017 15:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L347</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>221118-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>221121</Austr>
				<PresentationName>APO-Olmesartan HCTZ</PresentationName>
    			<PresentionStrength>40mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Olmesartan medoxomil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/07/2017 15:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L348</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>221121-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olmesartan medoxomil with hydrochlorothiazide (Organon)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>273576</Austr>
				<PresentationName>Olmesartan HCT - MYL</PresentationName>
    			<PresentionStrength>20mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olmesartan medoxomil,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Olmesartan HCT - MYL</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcohctm10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>olmesartan medoxomil with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2022-08-31 09:25:26.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 15:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C22</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>273576-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>273577</Austr>
				<PresentationName>Olmesartan HCT - MYL</PresentationName>
    			<PresentionStrength>40mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olmesartan medoxomil,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Olmesartan HCT - MYL</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcohctm10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>olmesartan medoxomil with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2022-08-31 09:25:26.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 15:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C23</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>273577-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>273578</Austr>
				<PresentationName>Olmesartan HCT - MYL</PresentationName>
    			<PresentionStrength>40mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olmesartan medoxomil,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Olmesartan HCT - MYL</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcohctm10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>olmesartan medoxomil with hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2022-08-31 09:25:26.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 15:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pinkish</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>273578-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olmesartan medoxomil with hydrochlorothiazide (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>221119</Austr>
				<PresentationName>Olmesartan/HCT Sandoz</PresentationName>
    			<PresentionStrength>20mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L</Side1Marking>
							<Side2Marking>346</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>221119-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>221124</Austr>
				<PresentationName>Olmesartan/HCT Sandoz</PresentationName>
    			<PresentionStrength>40mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L347</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>221124-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>221130</Austr>
				<PresentationName>Olmesartan/HCT Sandoz</PresentationName>
    			<PresentionStrength>40mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L348</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>221130-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olmetec</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>102138</Austr>
				<PresentationName>Olmetec</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olmesartan medoxomil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<QualiferData></QualiferData>
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						<ReleaseDate>2022-08-17 17:32:48.0</ReleaseDate>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>14/10/2010 12:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>C14</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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								<ViewLabel>C</ViewLabel>
								<ImageFileName>102138-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>102139</Austr>
				<PresentationName>Olmetec</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olmesartan medoxomil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<QualiferData></QualiferData>
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							<AvailableFormats>
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						<DateEffective>14/10/2010 12:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
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							<Side1Marking>C15</Side1Marking>
							<Side2Marking></Side2Marking>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Olmetec Plus</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>115661</Austr>
				<PresentationName>Olmetec Plus</PresentationName>
    			<PresentionStrength>40/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Olmesartan medoxomil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>21/10/2010 11:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
							<Colour>pinkish</Colour>
							<Scoring>unscored</Scoring>
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							<Side1Marking>C25</Side1Marking>
							<Side2Marking></Side2Marking>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>115737</Austr>
				<PresentationName>Olmetec Plus</PresentationName>
    			<PresentionStrength>40/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olmesartan medoxomil,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>21/10/2010 11:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish yellow</Colour>
							<Scoring>unscored</Scoring>
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							<Side1Marking>C23</Side1Marking>
							<Side2Marking></Side2Marking>
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								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>115738</Austr>
				<PresentationName>Olmetec Plus</PresentationName>
    			<PresentionStrength>20/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olmesartan medoxomil,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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						<DocumentName>Olmetec Plus</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
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							<Side2Marking></Side2Marking>
							<Views>
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			</Presentations>
		</Brand><Brand>
			<brandname>Omacor</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>155717</Austr>
				<PresentationName>Omacor</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Omega-3-acid ethyl esters 90</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<DocumentQualifiers>
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								<Format>PDF</Format>
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						<DateEffective>22/06/2011 11:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
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							<Colour>transparent and pale yellow</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
		</Brand><Brand>
			<brandname>Omepral</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>120594</Austr>
				<PresentationName>Omepral</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Omeprazole magnesium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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						<DateEffective>28/10/2008 15:16</DateEffective>
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							<DoseForm>Tablets</DoseForm>
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							<Side1Marking>20mG</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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		</Brand><Brand>
			<brandname>Omeprazole (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>159688</Austr>
				<PresentationName>Omeprazole AN</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Side1Marking></Side1Marking>
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			<isamtbrand>false</isamtbrand>
			<Presentations>
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				<PresentationName>APO-Omeprazole</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
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							<Colour>opaque yellow</Colour>
							<Scoring></Scoring>
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							<Side1Marking></Side1Marking>
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   				<WithdrawalDate>{ts '2022-10-21 00:00:00'}</WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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							<Side1Marking></Side1Marking>
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			<Presentations>
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			<Presentations>
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							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Side1Marking></Side1Marking>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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   				<WithdrawalDate></WithdrawalDate>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient></TGAIngredient>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient></TGAIngredient>
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							<Scoring></Scoring>
							<Shape></Shape>
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			<Presentations>
				<Austr>167314</Austr>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
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				<PresentationName>Onbrez Breezhaler</PresentationName>
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    			<PresentationForm>Inhalation capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
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							<View>
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								<ImageFileName>152188-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>300705</Austr>
				<PresentationName>Ondansetron Apotex</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>ondansetron hydrochloride dihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2022 10:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>BL</Side1Marking>
							<Side2Marking>8</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>300705-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>300710</Austr>
				<PresentationName>Ondansetron Apotex</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>ondansetron hydrochloride dihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2022 10:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>BL</Side1Marking>
							<Side2Marking>4</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>300710-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ondansetron (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>231602</Austr>
				<PresentationName>Ondansetron ODT GH</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/05/2017 17:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>O</Side1Marking>
							<Side2Marking>4</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>231602-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>231603</Austr>
				<PresentationName>Ondansetron ODT GH</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/05/2017 16:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>O</Side1Marking>
							<Side2Marking>8</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>231603-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ondansetron (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>163438</Austr>
				<PresentationName>Ondansetron SZ</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/07/2016 11:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>OND</Side1Marking>
							<Side2Marking>4</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>163438-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>163439</Austr>
				<PresentationName>Ondansetron SZ</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/07/2016 11:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>OND</Side1Marking>
							<Side2Marking>8</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>163439-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>163653</Austr>
				<PresentationName>Ondansetron SZ ODT</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/07/2016 11:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>O</Side1Marking>
							<Side2Marking>4</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>163653-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>163654</Austr>
				<PresentationName>Ondansetron SZ ODT</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/07/2016 11:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>O</Side1Marking>
							<Side2Marking>8</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>163654-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ondaz</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>116396</Austr>
				<PresentationName>Ondaz</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ondansetron hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 13:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>GX ET3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>116396-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>116415</Austr>
				<PresentationName>Ondaz</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ondansetron hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 13:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>GX ET5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>116415-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>116430</Austr>
				<PresentationName>Ondaz Zydis</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Wafers</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ondansetron</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 14:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Wafers</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>116430-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>116435</Austr>
				<PresentationName>Ondaz Zydis</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Wafers</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ondansetron</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 13:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Wafers</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>116435-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Onglyza</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>157907</Austr>
				<PresentationName>Onglyza</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Saxagliptin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Onglyza</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apcongly10219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>saxagliptin</ActiveIngredient>
						<ReleaseDate>2019-02-27 20:20:13.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/10/2014 10:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>4215</Side1Marking>
							<Side2Marking>5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157907-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>211214</Austr>
				<PresentationName>Onglyza</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Saxagliptin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Onglyza</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apcongly10219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>saxagliptin</ActiveIngredient>
						<ReleaseDate>2019-02-27 20:20:13.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>18/03/2015 11:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow to light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>4214</Side1Marking>
							<Side2Marking>2.5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>211214-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Onsetron</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>121359</Austr>
				<PresentationName>Onsetron</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 11:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121359-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121368</Austr>
				<PresentationName>Onsetron</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Side1Marking></Side1Marking>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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							<Side2Marking></Side2Marking>
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			<Presentations>
				<Austr>303071</Austr>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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							<PhaseItem>1</PhaseItem>
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							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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							<Side2Marking></Side2Marking>
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			<Presentations>
				<Austr>75034</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<brandname>Oroxine</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>125498</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
				<Austr>27535</Austr>
				<PresentationName>Orudis SR</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Side1Marking>ORUDIS SR 200</Side1Marking>
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			<Presentations>
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				<PresentationName>Oruvail SR</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ketoprofen</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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   				<WithdrawalDate></WithdrawalDate>
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							<Scoring>unscored</Scoring>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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				<PresentationName>Ossmax</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>beveled-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>227075-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>227076</Austr>
				<PresentationName>Osteomol</PresentationName>
    			<PresentionStrength>665mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2015 15:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>beveled-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>227076-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Otezla</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>220423</Austr>
				<PresentationName>Otezla</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>apremilast</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Otezla (ampremilast)</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ancapret11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>apremilast</ActiveIngredient>
						<ReleaseDate>2022-10-17 21:23:51.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/03/2022 10:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>diamond</Shape>
							<Side1Marking>APR</Side1Marking>
							<Side2Marking>30</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>220423-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>220424</Austr>
				<PresentationName>Otezla</PresentationName>
    			<PresentionStrength>Titration Pack</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>apremilast</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Otezla (ampremilast)</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ancapret11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>apremilast</ActiveIngredient>
						<ReleaseDate>2022-10-17 21:23:51.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/03/2022 10:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>diamond</Shape>
							<Side1Marking>APR</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>220424-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>diamond</Shape>
							<Side1Marking>APR</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>220424-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>3</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>diamond</Shape>
							<Side1Marking>APR</Side1Marking>
							<Side2Marking>30</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>220424-C03-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ovestin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>14514</Austr>
				<PresentationName>Ovestin</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oestriol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/10/2010 12:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DG 7</Side1Marking>
							<Side2Marking>ORGANON *</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>14514-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>35632</Austr>
				<PresentationName>Ovestin Ovula</PresentationName>
    			<PresentionStrength>0.5g</PresentionStrength>
    			<PresentationForm>Pessary</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient>Oestriol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/10/2010 12:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Pessary</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape>torpedo</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>35632-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Oxazepam (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>163213</Austr>
				<PresentationName>Apo-Oxazepam</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/10/2010 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>30</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>163213-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Oxybutynin Hydrochloride (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>130902</Austr>
				<PresentationName>Oxybutynin Sandoz</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-06-06 00:00:00'}</WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>oxybutynin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 16:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>130902-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Oxycodone hydrochloride (Mayne Pharma)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>225335</Austr>
				<PresentationName>Mayne Pharma Oxycodone IR</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Mayne Pharma Oxycodone IR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>oxycodone hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-11-30 11:36:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/01/2017 11:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>112</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>225335-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Oxycontin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>200024</Austr>
				<PresentationName>Oxycontin (reformulation)</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oxycodone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/09/2020 11:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ON</Side1Marking>
							<Side2Marking>40</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>200024-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>200025</Austr>
				<PresentationName>Oxycontin (reformulation)</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oxycodone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/09/2020 11:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ON</Side1Marking>
							<Side2Marking>30</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>200025-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>200026</Austr>
				<PresentationName>Oxycontin (reformulation)</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oxycodone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/09/2020 11:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>grey</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ON</Side1Marking>
							<Side2Marking>15</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>200026-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>200030</Austr>
				<PresentationName>Oxycontin (reformulation)</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oxycodone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/09/2020 11:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ON</Side1Marking>
							<Side2Marking>80</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>200030-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>200031</Austr>
				<PresentationName>Oxycontin (reformulation)</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oxycodone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/09/2020 11:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ON</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>200031-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>200033</Austr>
				<PresentationName>Oxycontin (reformulation)</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oxycodone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/09/2020 11:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ON</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>200033-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Oxynorm</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>74141</Austr>
				<PresentationName>OxyNorm</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oxycodone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/08/2010 09:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>pink and beige</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>ONR</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>74141-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>74143</Austr>
				<PresentationName>OxyNorm</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oxycodone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/08/2010 09:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and beige</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>ONR</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>74143-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>74145</Austr>
				<PresentationName>OxyNorm</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oxycodone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/08/2010 09:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange and beige</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>ONR</Side1Marking>
							<Side2Marking>5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>74145-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ozcef</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>122376</Austr>
				<PresentationName>Ozcef</PresentationName>
    			<PresentionStrength>375mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/02/2009 12:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>CEFACLOR CD 375 MG</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>122376-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Oziclide</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>124592</Austr>
				<PresentationName>Oziclide MR</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/02/2009 12:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>G30</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>124592-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ozidal</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>148964</Austr>
				<PresentationName>Ozidal</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/02/2010 15:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>RSN 0.5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>148964-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>148967</Austr>
				<PresentationName>Ozidal</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/02/2010 15:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>RSN 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>148967-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>148968</Austr>
				<PresentationName>Ozidal</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/02/2010 15:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>RSN 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>148968-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>148969</Austr>
				<PresentationName>Ozidal</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/02/2010 15:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>RSN 3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>148969-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>148970</Austr>
				<PresentationName>Ozidal</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/02/2010 15:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>RSN 4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>148970-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ozlodip</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>141652</Austr>
				<PresentationName>Ozlodip</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/02/2010 15:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>A 13</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>141652-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>142081</Austr>
				<PresentationName>Ozlodip</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/02/2010 15:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>A 14</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>142081-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ozmep</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>149348</Austr>
				<PresentationName>Ozmep</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brownish</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>149348-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ozole</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>122901</Austr>
				<PresentationName>Ozole</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluconazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 09:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue/white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>RANBAXY</Side1Marking>
							<Side2Marking>RANBAXY</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>122901-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>122903</Austr>
				<PresentationName>Ozole</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluconazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 09:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue/white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>RANBAXY</Side1Marking>
							<Side2Marking>RANBAXY</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>122903-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>122904</Austr>
				<PresentationName>Ozole</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 09:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>RANBAXY</Side1Marking>
							<Side2Marking>RANBAXY</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>122904-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>122909</Austr>
				<PresentationName>Ozole</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluconazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 09:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>purple/white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>RANBAXY</Side1Marking>
							<Side2Marking>RANBAXY</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>122909-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ozpan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>151290</Austr>
				<PresentationName>Ozpan</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/03/2010 09:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>II</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151290-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>151291</Austr>
				<PresentationName>Ozpan</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/03/2010 09:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>IV</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151291-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ozvir</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>117380</Austr>
				<PresentationName>Ozvir</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 09:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>ACV</Side1Marking>
							<Side2Marking>200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>117380-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Panadeine Forte</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>73507</Austr>
				<PresentationName>Panadeine Forte</PresentationName>
    			<PresentionStrength>500mg/30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Paracetamol,Codeine phosphate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Panadeine Forte</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcpanaf11221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>codeine phosphate hemihydrate with paracetamol</ActiveIngredient>
						<ReleaseDate>2021-12-08 17:05:08.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>P F</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73507-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Panadol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>116619</Austr>
				<PresentationName>Panadol Osteo</PresentationName>
    			<PresentionStrength>665mg</PresentionStrength>
    			<PresentationForm>Caplets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>paracetamol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/03/2009 11:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Caplets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>8</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>116619-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>123657</Austr>
				<PresentationName>Panadol Rapid Handipak</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Caplets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/03/2009 16:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Caplets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>P</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>123657-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>13590</Austr>
				<PresentationName>Panadol</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Caplets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/03/2009 11:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Caplets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PANADOL</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>13590-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>13591</Austr>
				<PresentationName>Panadol Immediate Release</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/03/2009 11:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PANADOL</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>13591-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>13591-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>15486</Austr>
				<PresentationName>Children&apos;s Panadol Suppositories </PresentationName>
    			<PresentionStrength>125mg</PresentionStrength>
    			<PresentationForm>Suppositories</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Childrens Panadol Suppositories</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gccpasup21117</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>paracetamol</ActiveIngredient>
						<ReleaseDate>2018-10-10 14:50:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/03/2009 11:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Suppositories</DoseForm>
							<Colour>off-white to ivory</Colour>
							<Scoring></Scoring>
							<Shape>tear drop</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>15486-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>15487</Austr>
				<PresentationName>Children&apos;s Panadol Suppositories </PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Suppositories</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Childrens Panadol Suppositories</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gccpasup21117</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>paracetamol</ActiveIngredient>
						<ReleaseDate>2018-10-10 14:50:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/03/2009 11:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Suppositories</DoseForm>
							<Colour>off-white to ivory</Colour>
							<Scoring></Scoring>
							<Shape>tear drop</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>15487-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>15488</Austr>
				<PresentationName>Panadol Immediate Release</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Suppositories</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/03/2009 11:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Suppositories</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape>torpedo</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>15488-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>15509</Austr>
				<PresentationName>Panadol Rapid Soluble</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/03/2009 11:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Effervescent Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>15509-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>15509-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156874</Austr>
				<PresentationName>Panadol Cold &amp; Flu Plus Decongestant</PresentationName>
    			<PresentionStrength>500mg/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/03/2015 10:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>sun graphic</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156874-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>260264</Austr>
				<PresentationName>Panadol Osteo</PresentationName>
    			<PresentionStrength>665mg</PresentionStrength>
    			<PresentationForm>Caplets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>paracetamol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Panadol Osteo</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>paracetamol</ActiveIngredient>
						<ReleaseDate>2022-03-16 15:38:32.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/08/2022 10:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>8</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>260264-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>35521</Austr>
				<PresentationName>Panadol Sinus Relief Original Formula</PresentationName>
    			<PresentionStrength>500mg/30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Panadol Sinus Relief Original Formula</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gccsroft31217</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>paracetamol with pseudoephedrine hydrochloride</ActiveIngredient>
						<ReleaseDate>2018-05-08 15:13:44.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/09/2011 14:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PANADOL</Side1Marking>
							<Side2Marking>SINUS</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>35521-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>40932</Austr>
				<PresentationName>Panadol Immediate Release</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Gel Caps</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/03/2009 11:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Gel Caps</DoseForm>
							<Colour>slightly off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PANADOL</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>40932-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>49816</Austr>
				<PresentationName>Panadol</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/03/2009 11:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Soluble Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>49816-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>49816-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>57397</Austr>
				<PresentationName>Panadol Night</PresentationName>
    			<PresentionStrength>500mg/25mg</PresentionStrength>
    			<PresentationForm>Caplets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/03/2015 10:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PANADOL</Side1Marking>
							<Side2Marking>NIGHT</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>57397-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>78692</Austr>
				<PresentationName>Panadol Rapid</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Caplets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/03/2009 16:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Caplets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>P</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>78692-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>81007</Austr>
				<PresentationName>Panadol Immediate Release</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Mini Caps</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/03/2009 11:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Mini Caps</DoseForm>
							<Colour>green and white</Colour>
							<Scoring></Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>81007-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Panadol Night</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167596</Austr>
				<PresentationName>Panadol Night</PresentationName>
    			<PresentionStrength>500mg/25mg</PresentionStrength>
    			<PresentationForm>Caplets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/08/2022 10:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PANADOL</Side1Marking>
							<Side2Marking>NIGHT</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167596-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Panafcort</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>27957</Austr>
				<PresentationName>Panafcort</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Prednisone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/07/2009 08:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PN 25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>27957-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>27974</Austr>
				<PresentationName>Panafcort</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Prednisone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/07/2009 08:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PN 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>27974-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>39879</Austr>
				<PresentationName>Panafcort</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Prednisone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/07/2009 08:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PN 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>39879-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Panafcortelone</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>27960</Austr>
				<PresentationName>Panafcortelone</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Prednisolone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/07/2009 08:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PL 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>27960-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>27962</Austr>
				<PresentationName>Panafcortelone</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Prednisolone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/07/2009 08:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PL 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>27962-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>27964</Austr>
				<PresentationName>Panafcortelone</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Prednisolone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/07/2009 08:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PL 25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>27964-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Panamax</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>15490</Austr>
				<PresentationName>Panamax</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>paracetamol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Panamax</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcpanam11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>paracetamol</ActiveIngredient>
						<ReleaseDate>2021-11-03 13:03:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/07/2008 11:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PANAMAX</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>15490-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Panamax Co</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>62661</Austr>
				<PresentationName>Panamax Co</PresentationName>
    			<PresentionStrength>500mg/8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>codeine phosphate hemihydrate,Paracetamol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Panamax Co</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcpanac11221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>codeine phosphate hemihydrate with paracetamol</ActiveIngredient>
						<ReleaseDate>2021-12-08 21:58:16.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/07/2008 11:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PANAMAX CO.</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>62661-A01-01-BL600.jpg</ImageFileName>
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			<isamtbrand>true</isamtbrand>
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			<isamtbrand>true</isamtbrand>
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    			<PresentationForm>Tablets</PresentationForm>
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    			<TGAIngredient></TGAIngredient>
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							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
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			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pantoprazole (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>156334</Austr>
				<PresentationName>Apo-Pantoprazole</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-10-21 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pantoprazole sodium sesquihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>14/06/2012 10:26</DateEffective>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>40</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>156337</Austr>
				<PresentationName>APOTEX-Pantoprazole</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-10-21 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pantoprazole sodium sesquihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>04/03/2016 09:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
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			</Presentations>
			<Presentations>
				<Austr>156338</Austr>
				<PresentationName>APO-Pantoprazole</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-10-21 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pantoprazole sodium sesquihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
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						<DateEffective>14/06/2012 10:28</DateEffective>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>156339</Austr>
				<PresentationName>APO-Pantoprazole</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Pantoprazole sodium sesquihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
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			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
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    			<Container>blister pack</Container>
    			<TGAIngredient>Pantoprazole sodium sesquihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
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							<Shape>oval</Shape>
							<Side1Marking>40</Side1Marking>
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			<Presentations>
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    			<Container>bottle</Container>
    			<TGAIngredient>Pantoprazole sodium sesquihydrate</TGAIngredient>
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							<PhaseItem>1</PhaseItem>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pantoprazole sodium sesquihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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    			<Container>blister pack</Container>
    			<TGAIngredient>Pantoprazole sodium sesquihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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			<Presentations>
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							<Colour>yellow to pale yellow</Colour>
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							<Side1Marking></Side1Marking>
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			<Presentations>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
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							<Shape>oval</Shape>
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							<Side2Marking>APO</Side2Marking>
							<Views>
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			<Presentations>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
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							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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			<Presentations>
				<Austr>213718</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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    			<PresentionStrength>20mg</PresentionStrength>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
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			</Presentations>
			<Presentations>
				<Austr>158191</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
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							<Side2Marking></Side2Marking>
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			</Presentations>
		</Brand><Brand>
			<brandname>Pantoprazole (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>155114</Austr>
				<PresentationName>Pantoprazole GH</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
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							<Side2Marking></Side2Marking>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>155115</Austr>
				<PresentationName>Pantoprazole GH</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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								<ImageFileName>155115-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>183533</Austr>
				<PresentationName>Pharmacy Action Heartburn Relief</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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			</Presentations>
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			<brandname>Pantoprazole (Mylan)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>158202</Austr>
				<PresentationName>Pantoprazole MYL (formerly Salpraz)</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-09 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pantoprazole sodium sesquihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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						<DateEffective>07/11/2016 15:55</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>158203</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
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    			<Container>blister pack</Container>
    			<TGAIngredient>Pantoprazole sodium sesquihydrate</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>147362</Austr>
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    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
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			</Presentations>
		</Brand><Brand>
			<brandname>Pantoprazole (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>156333</Austr>
				<PresentationName>Terry White Chemists Pantoprazole</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pantoprazole sodium sesquihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>40</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
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								<ImageFileName>156333-C01-02-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156336</Austr>
				<PresentationName>Terry White Chemists Pantoprazole</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pantoprazole sodium sesquihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>213719</Austr>
				<PresentationName>Terry White Chemists Pantoprazole</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pantoprazole sodium sesquihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
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							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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			</Presentations>
			<Presentations>
				<Austr>213720</Austr>
				<PresentationName>Terry White Chemists Pantoprazole</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Views>
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			</Presentations>
		</Brand><Brand>
			<brandname>Paracetamol (AFT)</brandname>
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			<Presentations>
				<Austr>144463</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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		</Brand><Brand>
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			<Presentations>
				<Austr>230261</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
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			<brandname>Paracetamol/Codeine Phosphate/Phenylephrine/Chlorpheniramine (Generic Health)</brandname>
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			<Presentations>
				<Austr>208283</Austr>
				<PresentationName>Pharmacy Action Cold &amp; Flu Relief PE Day &amp; Night</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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							<Scoring>scored</Scoring>
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							<Scoring>scored</Scoring>
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							<Side2Marking></Side2Marking>
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			<brandname>Paracetamol/Codeine Phosphate/Pseudoephedrine (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>203095</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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							<View>
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    							<ImageFileName>203095-B01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Paracetamol/Codeine Phosphate/Pseudoephedrine/Chlorpheniramine (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>192702</Austr>
				<PresentationName>Pharmacy Action Cold &amp; Flu Relief Day &amp; Night</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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							</View>
							<View>
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    							<ImageFileName>192702-B01-01-BL600.jpg</ImageFileName>
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							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
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							<Side2Marking></Side2Marking>
							<Views>
							<View>
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								<ImageFileName>192702-A02-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>192702-B02-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Paracetamol/dextromethorphan/phenylephrine/chlorpheniramine (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>216158</Austr>
				<PresentationName>Pharmacy Action Cold &amp; Flu + Cough Day &amp; Night</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Capsules</DoseForm>
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							<Shape></Shape>
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							<Views>
							<View>
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							<PhaseItem>2</PhaseItem>
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							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
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							<View>
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		</Brand><Brand>
			<brandname>Paracetamol/Phenylephrine/Chlorpheniramine (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>191939</Austr>
				<PresentationName>Pharmacy Action Hayfever &amp; Sinus Pain Relief PE</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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		</Brand><Brand>
			<brandname>Paracetamol/Pseudoephedrine/Chlorpheniramine (Generic Health)</brandname>
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			<Presentations>
				<Austr>189868</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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							<Scoring>scored</Scoring>
							<Shape>round</Shape>
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							<View>
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		</Brand><Brand>
			<brandname>Paradex</brandname>
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			<Presentations>
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				<PresentationName>Paradex</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Dextropropoxyphene hydrochloride,Paracetamol</TGAIngredient>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
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			<brandname>Paralgin</brandname>
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			<Presentations>
				<Austr>100682</Austr>
				<PresentationName>Paralgin</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<View>
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			<Presentations>
				<Austr>155493</Austr>
				<PresentationName>Parapane (new formulation)</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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			<brandname>Parbezol</brandname>
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			<Presentations>
				<Austr>189756</Austr>
				<PresentationName>Parbezol</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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							<Shape>round</Shape>
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			</Presentations>
			<Presentations>
				<Austr>189757</Austr>
				<PresentationName>Parbezol</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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			<brandname>Pariet</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
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				<PresentationName>Pariet</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
				<Austr>76186</Austr>
				<PresentationName>Pariet</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Pariet</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jccparie11122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>rabeprazole sodium</ActiveIngredient>
						<ReleaseDate>2022-12-02 13:09:54.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/07/2008 12:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>E243</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>76186-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Parlodel</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>13367</Austr>
				<PresentationName>Parlodel</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bromocriptine mesylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Parlodel</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcploor10920</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>bromocriptine mesilate</ActiveIngredient>
						<ReleaseDate>2020-10-07 14:15:03.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/12/2008 12:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>X C</Side1Marking>
							<Side2Marking>SANDOZ</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>13367-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Parnate</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>60821</Austr>
				<PresentationName>Parnate</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/07/2009 12:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>60821-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Paroxetine (Actavis)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>154655</Austr>
				<PresentationName>GN-Paroxetine</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/12/2009 13:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PX 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154655-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Paroxetine (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>176975</Austr>
				<PresentationName>Paroxetine AN</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/10/2017 13:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>modified capsule-shaped</Shape>
							<Side1Marking>C</Side1Marking>
							<Side2Marking>56</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>176975-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Paroxetine (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>150212</Austr>
				<PresentationName>APO-Paroxetine</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Paroxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 12:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>150212-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Paroxetine (Ascent)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>129419</Austr>
				<PresentationName>Paroxetine-DP</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 13:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>129419-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Paroxetine (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>83104</Austr>
				<PresentationName>Chemmart Paroxetine</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Paroxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 15:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>83104-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Paroxetine (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>219043</Austr>
				<PresentationName>Paroxetine GH</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/05/2017 15:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PX 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>219043-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Paroxetine (GenRx)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>83103</Austr>
				<PresentationName>GenRx Paroxetine</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Paroxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 15:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>83103-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Paroxetine (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>82550</Austr>
				<PresentationName>Paroxetine Sandoz</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Paroxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 14:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PX 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82550-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>82551</Austr>
				<PresentationName>Paroxetine Sandoz</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Paroxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 14:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PX 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82551-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Paroxetine (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>83106</Austr>
				<PresentationName>Terry White Chemists Paroxetine</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Paroxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 15:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>83106-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Paroxetine (Winthrop)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>80984</Austr>
				<PresentationName>Paroxetine Winthrop</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Paroxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/07/2008 11:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PX 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>80984-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Paxam</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>54846</Austr>
				<PresentationName>Paxam</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Clonazepam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Paxam</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcpaxam10619</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clonazepam</ActiveIngredient>
						<ReleaseDate>2019-06-07 14:27:54.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CN 0.5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>54846-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>54847</Austr>
				<PresentationName>Paxam</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Clonazepam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Paxam</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcpaxam10619</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clonazepam</ActiveIngredient>
						<ReleaseDate>2019-06-07 14:27:54.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CN 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>54847-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Paxtine</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>227120</Austr>
				<PresentationName>Paxtine</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Paroxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Paxtine</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcpaxti10621</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>paroxetine hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-06-29 09:28:49.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/12/2018 11:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>P 2</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>227120-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pemzo</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167315</Austr>
				<PresentationName>Pemzo</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167315-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Penta-Vite</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>115419</Austr>
				<PresentationName>Penta-Vite</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2009 14:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink/brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>teddy bear shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>115419-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pentasa</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>164142</Austr>
				<PresentationName>Pentasa</PresentationName>
    			<PresentionStrength>1g</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mesalazine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Pentasa Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fpcpentt10721</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>mesalazine</ActiveIngredient>
						<ReleaseDate>2021-07-05 17:43:29.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/08/2010 14:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white grey to pale brown speckled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>PENTASA</Side1Marking>
							<Side2Marking>PENTASA</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>164142-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>98034</Austr>
				<PresentationName>Pentasa</PresentationName>
    			<PresentionStrength>1g</PresentionStrength>
    			<PresentationForm>Suppositories</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mesalazine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Pentasa Suppositories</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fpcpents10721</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>mesalazine</ActiveIngredient>
						<ReleaseDate>2021-07-05 17:41:16.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/10/2010 08:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Suppositories</DoseForm>
							<Colour>white to tan spotted</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>98034-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>99139</Austr>
				<PresentationName>Pentasa</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mesalazine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Pentasa Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>fpcpentt10721</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>mesalazine</ActiveIngredient>
						<ReleaseDate>2021-07-05 17:43:29.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/09/2008 14:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white grey to pale brown specked</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PENTASA</Side1Marking>
							<Side2Marking>500 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>99139-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>99139-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pepzan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>67944</Austr>
				<PresentationName>Pepzan</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 13:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>square</Shape>
							<Side1Marking>40</Side1Marking>
							<Side2Marking>dp</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>67944-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Periactin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>62384</Austr>
				<PresentationName>Periactin</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>cyproheptadine hydrochloride sesquihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Periactin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocperin11121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>cyproheptadine hydrochloride sesquihydrate</ActiveIngredient>
						<ReleaseDate>2021-11-22 08:14:05.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/12/2010 11:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>P4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62384-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Perindo</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>121747</Austr>
				<PresentationName>Perindo</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Perindopril erbumine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Perindo</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcperin10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>perindopril</ActiveIngredient>
						<ReleaseDate>2022-07-06 10:24:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121747-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121748</Austr>
				<PresentationName>Perindo</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Perindopril erbumine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Perindo</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcperin10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>perindopril</ActiveIngredient>
						<ReleaseDate>2022-07-06 10:24:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>rod-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121748-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121749</Austr>
				<PresentationName>Perindo</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Perindopril erbumine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Perindo</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcperin10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>perindopril</ActiveIngredient>
						<ReleaseDate>2022-07-06 10:24:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>heart</Side1Marking>
							<Side2Marking>Servier logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121749-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Perindo Combi</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>114207</Austr>
				<PresentationName>Perindo Combi</PresentationName>
    			<PresentionStrength>4mg/1.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Indapamide hemihydrate,Perindopril erbumine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Perindo Combi</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcperco10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>perindopril with indapamide hemihydrate</ActiveIngredient>
						<ReleaseDate>2022-07-06 10:25:51.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rod-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>114207-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Perindopril Arginine (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>184806</Austr>
				<PresentationName>APO-Perindopril Arginine</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>perindopril arginine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/12/2016 10:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>P 5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184806-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>184808</Austr>
				<PresentationName>APO-Perindopril Arginine </PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>perindopril arginine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/12/2016 10:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>2.5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184808-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>184812</Austr>
				<PresentationName>APO-Perindopril Arginine </PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>perindopril arginine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/12/2016 10:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>P 10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184812-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Perindopril Arginine-Amlodipine (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>224292</Austr>
				<PresentationName>APO-Perindopril Arginine/Amlodipine</PresentationName>
    			<PresentionStrength>5mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>amlodipine besilate,perindopril arginine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/05/2017 13:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>square</Shape>
							<Side1Marking>5/10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>224292-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>224300</Austr>
				<PresentationName>APO-Perindopril Arginine/Amlodipine</PresentationName>
    			<PresentionStrength>10mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>amlodipine besilate,perindopril arginine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/05/2017 13:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>10/10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>224300-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>224306</Austr>
				<PresentationName>APO-Perindopril Arginine/Amlodipine</PresentationName>
    			<PresentionStrength>5mg/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>amlodipine besilate,perindopril arginine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/05/2017 13:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>5/5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>224306-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>224316</Austr>
				<PresentationName>APO-Perindopril Arginine/Amlodipine</PresentationName>
    			<PresentionStrength>10mg/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>amlodipine besilate,perindopril arginine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/05/2017 13:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>triangular</Shape>
							<Side1Marking>10/5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>224316-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Perindopril Erbumine (AN)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>212715</Austr>
				<PresentationName>Perindopril AN</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 14:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>212715-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>212716</Austr>
				<PresentationName>Perindopril AN</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 14:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>rod-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>212716-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>212717</Austr>
				<PresentationName>Perindopril AN</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 14:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>heart</Side1Marking>
							<Side2Marking>logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>212717-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Perindopril erbumine (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>151911</Austr>
				<PresentationName>APO-Perindopril</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Perindopril erbumine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/10/2010 11:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PE2</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151911-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>151912</Austr>
				<PresentationName>APO-Perindopril</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Perindopril erbumine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/10/2010 11:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PE 4</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151912-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>151913</Austr>
				<PresentationName>APO-Perindopril</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Perindopril erbumine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/10/2010 11:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PE 8</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151913-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Perindopril Erbumine (Blooms The Chemist)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>151914</Austr>
				<PresentationName>Blooms The Chemist Perindopril </PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Perindopril erbumine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/09/2015 11:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PE2</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151914-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>151915</Austr>
				<PresentationName>Blooms The Chemist Perindopril </PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Perindopril erbumine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/09/2015 11:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PE 4</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151915-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>151916</Austr>
				<PresentationName>Blooms The Chemist Perindopril </PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Perindopril erbumine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/09/2015 11:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PE 8</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151916-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Perindopril erbumine (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>121628</Austr>
				<PresentationName>Chemmart Perindopril</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Perindopril erbumine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 15:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PE2</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121628-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121629</Austr>
				<PresentationName>Chemmart Perindopril</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Perindopril erbumine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 15:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PE 4</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121629-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121630</Austr>
				<PresentationName>Chemmart Perindopril</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Perindopril erbumine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 15:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PE 8</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121630-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Perindopril Erbumine (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>125455</Austr>
				<PresentationName>Perindopril generichealth</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>4 4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>125455-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>125456</Austr>
				<PresentationName>Perindopril generichealth</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>8</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>125456-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Perindopril erbumine (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>121631</Austr>
				<PresentationName>Terry White Chemists Perindopril</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Perindopril erbumine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 15:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PE2</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121631-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121632</Austr>
				<PresentationName>Terry White Chemists Perindopril</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Perindopril erbumine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 15:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PE 4</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121632-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121633</Austr>
				<PresentationName>Terry White Chemists Perindopril</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Perindopril erbumine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 15:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PE 8</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121633-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Perindopril Erbumine/Indapamide Hemihydrate (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>147136</Austr>
				<PresentationName>Perindopril and Indapamide Hemihydrate CH</PresentationName>
    			<PresentionStrength>4mg/1.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/10/2017 13:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>147136-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Perindopril Erbumine/Indapamide Hemihydrate (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>127120</Austr>
				<PresentationName>Chemmart Perindopril/Indapamide</PresentationName>
    			<PresentionStrength>4mg/1.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Indapamide hemihydrate,Perindopril erbumine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/06/2009 09:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>4/1.25</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127120-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Perindopril Erbumine/Indapamide Hemihydrate (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>147149</Austr>
				<PresentationName>Perindopril/Indapamide GH 4/1.25</PresentationName>
    			<PresentionStrength>4mg/1.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2015 15:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>147149-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Perindopril Erbumine/Indapamide Hemihydrate (GenRx)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>127119</Austr>
				<PresentationName>GenRx Perindopril / Indapamide</PresentationName>
    			<PresentionStrength>4mg/1.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Perindopril erbumine,Indapamide hemihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/07/2008 08:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>4/1.25</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127119-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Perindopril Erbumine/Indapamide Hemihydrate (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>127121</Austr>
				<PresentationName>Terry White Chemists Perindopril/Indapamide</PresentationName>
    			<PresentionStrength>4mg/1.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Indapamide hemihydrate,Perindopril erbumine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/06/2009 09:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>4/1.25</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127121-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Permax</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>49024</Austr>
				<PresentationName>Permax</PresentationName>
    			<PresentionStrength>50mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pergolide mesylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/11/2008 11:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>ivory</Colour>
							<Scoring>scored</Scoring>
							<Shape>rectangular-shaped</Shape>
							<Side1Marking>0.05</Side1Marking>
							<Side2Marking>square logo square logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>49024-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>49026</Austr>
				<PresentationName>Permax</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pergolide mesylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/11/2008 11:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>rectangular-shaped</Shape>
							<Side1Marking>1</Side1Marking>
							<Side2Marking>square logo square logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>49026-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>93396</Austr>
				<PresentationName>Permax</PresentationName>
    			<PresentionStrength>250mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pergolide mesylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/11/2008 11:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>scored</Scoring>
							<Shape>rectangular-shaped</Shape>
							<Side1Marking>0.25</Side1Marking>
							<Side2Marking>square logo square logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>93396-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pexsig</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>52182</Austr>
				<PresentationName>Pexsig</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PEXSIG</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>52182-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pharmacor AmoxyClav</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>196892</Austr>
				<PresentationName>Pharmacor AmoxyClav</PresentationName>
    			<PresentionStrength>500mg/125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/10/2013 11:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>196892-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pharmacor Citalo</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>158873</Austr>
				<PresentationName>Pharmacor Citalo</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/10/2013 11:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>BL</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158873-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pharmacor Prozine</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>172127</Austr>
				<PresentationName>Pharmacor Prozine</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/12/2013 15:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>172127-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pharmacor Stomach Ease</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>138000</Austr>
				<PresentationName>Pharmacor Stomach Ease</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/08/2009 12:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>138000-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Phenergan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>80159</Austr>
				<PresentationName>Phenergan</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>promethazine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Phenergan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcphene10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>promethazine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-06-14 15:46:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PN 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>80159-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>80160</Austr>
				<PresentationName>Phenergan</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>promethazine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Phenergan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcphene10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>promethazine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-06-14 15:46:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PN 25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>80160-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Phenobarb</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>19758</Austr>
				<PresentationName>Phenobarbitone Aspen</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/04/2012 14:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>19758-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Phosphate-Sandoz</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>13368</Austr>
				<PresentationName>Phosphate-Sandoz</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>tube</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/12/2008 10:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>13368-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>13368-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Physeptone</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>76083</Austr>
				<PresentationName>Physeptone Tablets</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 15:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>WELLCOME U4B</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>76083-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Physiotens</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>114119</Austr>
				<PresentationName>Physiotens</PresentationName>
    			<PresentionStrength>0.2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Moxonidine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Physiotens</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocphysi10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>moxonidine</ActiveIngredient>
						<ReleaseDate>2022-02-17 13:26:53.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/09/2008 15:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>0.2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>114119-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>114121</Austr>
				<PresentationName>Physiotens</PresentationName>
    			<PresentionStrength>0.4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Moxonidine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Physiotens</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocphysi10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>moxonidine</ActiveIngredient>
						<ReleaseDate>2022-02-17 13:26:53.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/09/2008 15:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dull red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>0.4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>114121-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Piax</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>168926</Austr>
				<PresentationName>Piax</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Clopidogrel hydrogen sulfate</TGAIngredient>
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			<Presentations>
				<Austr>168927</Austr>
				<PresentationName>Piax</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clopidogrel hydrogen sulfate</TGAIngredient>
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				<Documents>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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			<brandname>Piax Plus Asprin</brandname>
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				<Austr>219059</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient></TGAIngredient>
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							<DoseForm>Tablets</DoseForm>
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							<Side1Marking>CL 7</Side1Marking>
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		</Brand><Brand>
			<brandname>Pioglitazone (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>176381</Austr>
				<PresentationName>Pioglitazone AN</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pioglitazone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>13/03/2019 14:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>H</Side1Marking>
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							<Views>
							<View>
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								<ImageFileName>176381-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>176387</Austr>
				<PresentationName>Pioglitazone AN</PresentationName>
    			<PresentionStrength>45mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pioglitazone hydrochloride</TGAIngredient>
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					<Versions>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
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							<Shape>round</Shape>
							<Side1Marking>H</Side1Marking>
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							<Views>
							<View>
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								<ImageFileName>176387-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>176388</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pioglitazone hydrochloride</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>H</Side1Marking>
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							<Views>
							<View>
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			</Presentations>
		</Brand><Brand>
			<brandname>Pioglitazone (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>166911</Austr>
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    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Pioglitazone hydrochloride</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>15</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166911-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>166913</Austr>
				<PresentationName>Apotex-Pioglitazone</PresentationName>
    			<PresentionStrength>45mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Pioglitazone hydrochloride</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateEffective>31/05/2011 09:42</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>45</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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								<ImageFileName>166913-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>166914</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Pioglitazone hydrochloride</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>31/05/2011 09:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>30</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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								<ImageFileName>166914-C01-01-BL600.jpg</ImageFileName>
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			<brandname>Pioglitazone (GA)</brandname>
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			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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		</Brand><Brand>
			<brandname>Pioglitazone (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>156715</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
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                    	<Phase>
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							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PIO</Side1Marking>
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							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>156716</Austr>
				<PresentationName>Pharmacor Pioglitazone</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PIO</Side1Marking>
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							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>156718</Austr>
				<PresentationName>Pharmacor Pioglitazone</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PIO</Side1Marking>
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							<Views>
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			<brandname>Pioglitazone (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>162222</Austr>
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    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pioglitazone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PGT 30</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>162222-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>162223</Austr>
				<PresentationName>Pioglitazone Sandoz</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pioglitazone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PGT 15</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>162223-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>162225</Austr>
				<PresentationName>Pioglitazone Sandoz</PresentationName>
    			<PresentionStrength>45mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pioglitazone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PGT 45</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>162225-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Piqray</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>315020</Austr>
				<PresentationName>Piqray</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>alpelisib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Piqray</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcpiqor10221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>alpelisib</ActiveIngredient>
						<ReleaseDate>2021-11-01 13:17:16.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/08/2022 13:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>ovaloid</Shape>
							<Side1Marking>YL7</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>315020-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>315055</Austr>
				<PresentationName>Piqray</PresentationName>
    			<PresentionStrength>250mg (200mg+50mg)</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>alpelisib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Piqray</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcpiqor10221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>alpelisib</ActiveIngredient>
						<ReleaseDate>2021-11-01 13:17:16.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/08/2022 13:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>ovaloid</Shape>
							<Side1Marking>YL7</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>315055-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>L7</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>315055-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>315064</Austr>
				<PresentationName>Piqray</PresentationName>
    			<PresentionStrength>300mg (150mgx2)</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>alpelisib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Piqray</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcpiqor10221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>alpelisib</ActiveIngredient>
						<ReleaseDate>2021-11-01 13:17:16.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/08/2022 13:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>ovaloid</Shape>
							<Side1Marking>UL7</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>315064-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Piroxicam (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>75039</Austr>
				<PresentationName>APO-Piroxicam</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Piroxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/08/2008 09:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>maroon/blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75039-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>75043</Austr>
				<PresentationName>APO-Piroxicam</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Piroxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/08/2008 11:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light maroon and dark maroon</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75043-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Piroxicam (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>75037</Austr>
				<PresentationName>Chemmart Piroxicam</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Piroxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/08/2008 09:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>maroon/blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75037-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>75041</Austr>
				<PresentationName>Chemmart Piroxicam</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Piroxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/08/2008 11:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light maroon and dark maroon</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75041-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Piroxicam (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>75036</Austr>
				<PresentationName>Terry White Chemists Piroxicam</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Piroxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/08/2008 09:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>maroon/blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75036-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>75040</Austr>
				<PresentationName>Terry White Chemists Piroxicam</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Piroxicam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 13:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light maroon and dark maroon</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75040-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pizaccord</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>156719</Austr>
				<PresentationName>Pizaccord</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/09/2011 09:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PIO</Side1Marking>
							<Side2Marking>30</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156719-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156722</Austr>
				<PresentationName>Pizaccord</PresentationName>
    			<PresentionStrength>45mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/09/2011 09:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PIO</Side1Marking>
							<Side2Marking>45</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156722-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156723</Austr>
				<PresentationName>Pizaccord</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/09/2011 09:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PIO</Side1Marking>
							<Side2Marking>15</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156723-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Placil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>143879</Austr>
				<PresentationName>Placil</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clomipramine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Placil</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcplaci10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clomipramine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-06-14 11:44:06.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Cl 25</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>143879-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Plaquenil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>50055</Austr>
				<PresentationName>Plaquenil</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Hydroxychloroquine sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Plaquenil</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcplaqu11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>hydroxychloroquine sulfate</ActiveIngredient>
						<ReleaseDate>2022-11-02 16:46:19.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>peanut-shaped</Shape>
							<Side1Marking>PLAQUENIL</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>50055-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Plavicor</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>187039</Austr>
				<PresentationName>Plavicor</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/10/2012 14:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CI</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>187039-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Plavix</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>151257</Austr>
				<PresentationName>Plavix</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clopidogrel hydrogen sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Plavix</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcplavi10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>clopidogrel </ActiveIngredient>
						<ReleaseDate>2022-07-28 15:42:11.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/02/2010 14:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>1332</Side1Marking>
							<Side2Marking>300</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151257-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>78622</Austr>
				<PresentationName>Plavix</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clopidogrel hydrogen sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/06/2008 14:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>75</Side1Marking>
							<Side2Marking>1171</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>78622-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Plendil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>51774</Austr>
				<PresentationName>Plendil ER</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Felodipine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Plendil ER</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apcplend10517</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>felodipine</ActiveIngredient>
						<ReleaseDate>2017-05-30 09:51:10.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 11:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>A FL</Side1Marking>
							<Side2Marking>2.5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>51774-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>51775</Austr>
				<PresentationName>Plendil ER</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Felodipine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Plendil ER</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apcplend10517</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>felodipine</ActiveIngredient>
						<ReleaseDate>2017-05-30 09:51:10.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 11:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>A FM</Side1Marking>
							<Side2Marking>5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>51775-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>51776</Austr>
				<PresentationName>Plendil ER</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Felodipine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Plendil ER</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apcplend10517</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>felodipine</ActiveIngredient>
						<ReleaseDate>2017-05-30 09:51:10.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 11:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red-brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>A FE</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>51776-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Plidogrel</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>218326</Austr>
				<PresentationName>Plidogrel</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>218326-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Polaramine</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>154653</Austr>
				<PresentationName>Polaramine</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>05/01/2011 16:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Flask and bowl logo</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154653-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ponstan (Pfizer)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>14387</Austr>
				<PresentationName>Ponstan</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Mefenamic acid</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>ivory opaque and aqua blue opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>PARKE DAVIS</Side1Marking>
							<Side2Marking>PARKE DAVIS</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>14387-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>225658</Austr>
				<PresentationName>Ponstan</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mefenamic acid</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Ponstan</DocumentName>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>mefenamic acid</ActiveIngredient>
						<ReleaseDate>2022-11-07 13:25:38.0</ReleaseDate>
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				<Images>
					<Versions>
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						<VersionStatus>Current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>ivory opaque and aqua blue opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>PARKE DAVIS</Side1Marking>
							<Side2Marking>PARKE DAVIS</Side2Marking>
							<Views>
							<View>
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								<ImageFileName>225658-C01-01-BL600.jpg</ImageFileName>
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		</Brand><Brand>
			<brandname>Postella-1</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>231505</Austr>
				<PresentationName>Postella-1</PresentationName>
    			<PresentionStrength>1.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</View>
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						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>238206</Austr>
				<PresentationName>Postella-1</PresentationName>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/06/2019 06:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white or nearly white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>cylindrical</Shape>
							<Side1Marking>210</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>225631-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pramipexole (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>225580</Austr>
				<PresentationName>APO-Pramipexole ER</PresentationName>
    			<PresentionStrength>1.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>pramipexole dihydrochloride monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 19:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white or nearly white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>cylindrical</Shape>
							<Side1Marking>105</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>225580-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>225586</Austr>
				<PresentationName>APO-Pramipexole ER</PresentationName>
    			<PresentionStrength>2.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>pramipexole dihydrochloride monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 19:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white or nearly white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>cylindrical</Shape>
							<Side1Marking>157</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>225586-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>225597</Austr>
				<PresentationName>APO-Pramipexole ER</PresentationName>
    			<PresentionStrength>4.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>pramipexole dihydrochloride monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 19:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white or nearly white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>cylindrical</Shape>
							<Side1Marking>315</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>225597-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>225621</Austr>
				<PresentationName>APO-Pramipexole ER</PresentationName>
    			<PresentionStrength>0.75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>pramipexole dihydrochloride monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 19:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white or nearly white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>cylindrical</Shape>
							<Side1Marking>052</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>225621-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>225622</Austr>
				<PresentationName>APO-Pramipexole ER</PresentationName>
    			<PresentionStrength>0.375mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>pramipexole dihydrochloride monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 19:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white or nearly white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>cylindrical</Shape>
							<Side1Marking>026</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>225622-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>225625</Austr>
				<PresentationName>APO-Pramipexole ER</PresentationName>
    			<PresentionStrength>3.75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>pramipexole dihydrochloride monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 19:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white or nearly white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>cylindrical</Shape>
							<Side1Marking>262</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>225625-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>225627</Austr>
				<PresentationName>APO-Pramipexole ER</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>pramipexole dihydrochloride monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 19:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white or nearly white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>cylindrical</Shape>
							<Side1Marking>210</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>225627-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>227666</Austr>
				<PresentationName>APO-Pramipexole </PresentationName>
    			<PresentionStrength>0.125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/04/2019 18:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>227666-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>227667</Austr>
				<PresentationName>APO-Pramipexole</PresentationName>
    			<PresentionStrength>0.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/04/2019 18:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>B</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>227667-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>227669</Austr>
				<PresentationName>APO-Pramipexole</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/04/2019 18:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>D</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>227669-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pramipexole (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>214453</Austr>
				<PresentationName>Pramipexole GH</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/05/2017 15:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CL 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214453-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>214456</Austr>
				<PresentationName>Pramipexole GH</PresentationName>
    			<PresentionStrength>0.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/05/2017 15:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>CL 3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214456-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>214463</Austr>
				<PresentationName>Pramipexole GH</PresentationName>
    			<PresentionStrength>0.125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/05/2017 15:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>CL</Side1Marking>
							<Side2Marking>2</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214463-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pravachol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>58075</Austr>
				<PresentationName>Pravachol</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>58075-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>68704</Austr>
				<PresentationName>Pravachol</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>68704-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>68706</Austr>
				<PresentationName>Pravachol</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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							<DoseForm>Tablets</DoseForm>
							<Colour>yellow mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
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							<Views>
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			</Presentations>
			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
							<Colour>yellow mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>R</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
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								<ImageFileName>191714-C01-01-BL600.jpg</ImageFileName>
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			<Presentations>
				<Austr>191718</Austr>
				<PresentationName>Pravastatin AN</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>13/10/2017 14:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>yellow mottled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>R</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>191718-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pravastatin Sodium (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>118735</Austr>
				<PresentationName>Apo-Pravastatin</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pravastatin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PRA 10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>118735-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>118736</Austr>
				<PresentationName>Apo-Pravastatin</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pravastatin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white to light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PRA 20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>118736-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>118737</Austr>
				<PresentationName>Apo-Pravastatin</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pravastatin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/12/2010 12:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PRA 40</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>118737-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>145169</Austr>
				<PresentationName>Apo-Pravastatin</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pravastatin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/12/2010 12:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white to light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PRA 80</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>145169-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>145178</Austr>
				<PresentationName>Apo-Pravastatin</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Pravastatin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white to light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PRA 80</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>145178-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166255</Austr>
				<PresentationName>Apo-Pravastatin</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Pravastatin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/12/2010 12:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PRA 10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166255-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166256</Austr>
				<PresentationName>Apo-Pravastatin</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Pravastatin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white to light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PRA 20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166256-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166257</Austr>
				<PresentationName>Apo-Pravastatin</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Pravastatin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PRA 40</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166257-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Pravastatin Sodium (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>139595</Austr>
				<PresentationName>Pravastatin generichealth</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>139595-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
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			</Presentations>
			<Presentations>
				<Austr>139600</Austr>
				<PresentationName>Pravastatin generichealth</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>139600-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>139601</Austr>
				<PresentationName>Pravastatin generichealth</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>139601-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>139602</Austr>
				<PresentationName>Pravastatin generichealth</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>PRV</Side1Marking>
							<Side2Marking>80</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>139602-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pravastatin Sodium (GenRx)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>118646</Austr>
				<PresentationName>GenRx Pravastatin</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pravastatin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PRA 10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>118646-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>118650</Austr>
				<PresentationName>GenRx Pravastatin</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pravastatin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/08/2008 09:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white to light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PRA 20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>118650-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>118661</Austr>
				<PresentationName>GenRx Pravastatin</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pravastatin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/08/2008 09:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PRA 40</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>118661-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pravastatin Sodium (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>156357</Austr>
				<PresentationName>Pharmacor Pravastat</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/11/2011 11:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rounded rectangular</Shape>
							<Side1Marking>PDT</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156357-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156358</Austr>
				<PresentationName>Pharmacor Pravastat</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/11/2011 11:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rounded rectangular</Shape>
							<Side1Marking>PDT</Side1Marking>
							<Side2Marking>40</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156358-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156364</Austr>
				<PresentationName>Pharmacor Pravastat</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/11/2011 11:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rounded rectangular</Shape>
							<Side1Marking>PDT</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156364-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pravastatin Sodium (Sandoz)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>152450</Austr>
				<PresentationName>Pravastatin Sandoz</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pravastatin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 12:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light brown</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>P 40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152450-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>152451</Austr>
				<PresentationName>Pravastatin Sandoz</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pravastatin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 12:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light brown</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>P 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152451-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>152452</Austr>
				<PresentationName>Pravastatin Sandoz</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pravastatin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 12:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>HLP 80</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152452-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>152458</Austr>
				<PresentationName>Pravastatin Sandoz</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pravastatin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 12:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light brown</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>P 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152458-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Prazosin (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>73858</Austr>
				<PresentationName>APO-Prazosin</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Prazosin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/10/2008 15:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>APO P1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73858-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>73862</Austr>
				<PresentationName>APO-Prazosin</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Prazosin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/10/2008 15:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>APO P2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73862-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>73866</Austr>
				<PresentationName>APO-Prazosin</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Prazosin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/10/2008 15:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>diamond-shaped</Shape>
							<Side1Marking>APO P5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73866-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Predsolone</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>99791</Austr>
				<PresentationName>Predsolone</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Prednisolone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/11/2008 13:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PL 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>99791-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Predsone</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>99792</Austr>
				<PresentationName>Predsone</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Prednisolone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<DateEffective>08/07/2009 08:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PN 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>99792-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pregabalin (Alphapharm)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>224416</Austr>
				<PresentationName>Pregabalin Alphapharm (formerly Lyzalon)</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pregabalin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<QualiferData></QualiferData>
						<DocumentName>Pregabalin Alphapharm (formerly Lyzalon)</DocumentName>
						<DocumentTypes>
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								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>pregabalin</ActiveIngredient>
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						<DateEffective>25/06/2019 06:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light peach opaque and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>MYLAN PB 300</Side1Marking>
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							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>224435</Austr>
				<PresentationName>Pregabalin Alphapharm (formerly Lyzalon)</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentTypes>
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							<AvailableFormats>
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							<PhaseItem>1</PhaseItem>
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							<Shape></Shape>
							<Side1Marking>MYLAN PB 25</Side1Marking>
							<Side2Marking>MYLAN PB 25</Side2Marking>
							<Views>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>224436</Austr>
				<PresentationName>Pregabalin Alphapharm (formerly Lyzalon)</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pregabalin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Pregabalin Alphapharm (formerly Lyzalon)</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>pregabalin</ActiveIngredient>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
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							<Scoring></Scoring>
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							<Side1Marking>MYLAN PB 75</Side1Marking>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>224446</Austr>
				<PresentationName>Pregabalin Alphapharm (formerly Lyzalon)</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pregabalin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>pregabalin</ActiveIngredient>
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							<Side1Marking>MYLAN PB150</Side1Marking>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pregabalin (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>193255</Austr>
				<PresentationName>APO-Pregabalin</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pregabalin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/11/2017 11:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>P25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>193255-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>193274</Austr>
				<PresentationName>APO-Pregabalin</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pregabalin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/11/2017 11:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>P75</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>193274-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
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			</Presentations>
			<Presentations>
				<Austr>193276</Austr>
				<PresentationName>APO-Pregabalin</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pregabalin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>16/11/2017 11:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>P150</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>193276-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
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			</Presentations>
			<Presentations>
				<Austr>193279</Austr>
				<PresentationName>APO-Pregabalin</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pregabalin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>16/11/2017 11:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>P300</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>193279-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>267552</Austr>
				<PresentationName>Pregabalin Apotex</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
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						<DateEffective>03/03/2020 22:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light grey</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>267552-C01-02-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>267554</Austr>
				<PresentationName>Pregabalin Apotex</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>03/03/2020 22:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light red and light grey</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>75</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>267554-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>267556</Austr>
				<PresentationName>Pregabalin Apotex</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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						<VersionSequence>1</VersionSequence>
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							<PhaseItem>1</PhaseItem>
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							<Colour>light grey</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
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								<ViewLabel>C</ViewLabel>
								<ImageFileName>267556-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>267559</Austr>
				<PresentationName>Pregabalin Apotex</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red and light grey</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>300</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>267559-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pregabalin (Blooms the Chemist)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>193298</Austr>
				<PresentationName>Blooms the Chemist Pregabalin </PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pregabalin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
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							<Side1Marking>APO</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>193298-C01-01-BL600.jpg</ImageFileName>
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			<Presentations>
				<Austr>193300</Austr>
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    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pregabalin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>26/09/2018 16:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>P75</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>193300-C01-01-BL600.jpg</ImageFileName>
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			<Presentations>
				<Austr>193302</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pregabalin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>P150</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>193302-C01-01-BL600.jpg</ImageFileName>
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			<Presentations>
				<Austr>193305</Austr>
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    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pregabalin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>P300</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>193305-C01-01-BL600.jpg</ImageFileName>
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			<Presentations>
				<Austr>267471</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
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							<Colour>light grey</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>150</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>267471-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>267477</Austr>
				<PresentationName>BTC Pregabalin</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/04/2019 19:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red and light grey</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>300</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>267477-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pregabalin (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>210043</Austr>
				<PresentationName>Pregabalin Sandoz</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pregabalin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>210043-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>210046</Austr>
				<PresentationName>Pregabalin Sandoz</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pregabalin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>210046-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>210049</Austr>
				<PresentationName>Pregabalin Sandoz</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pregabalin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>skin</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>210049-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>210050</Austr>
				<PresentationName>Pregabalin Sandoz</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pregabalin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red and skin</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>210050-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Premarin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>177673</Austr>
				<PresentationName>Premarin</PresentationName>
    			<PresentionStrength>0.3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oestrogens - conjugated</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Premarin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcpremt10220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>conjugated estrogens</ActiveIngredient>
						<ReleaseDate>2020-03-09 11:02:23.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/03/2013 14:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>0.3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>177673-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>177674</Austr>
				<PresentationName>Premarin</PresentationName>
    			<PresentionStrength>0.625mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oestrogens - conjugated</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Premarin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcpremt10220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>conjugated estrogens</ActiveIngredient>
						<ReleaseDate>2020-03-09 11:02:23.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/03/2013 14:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>maroon</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>0.625</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>177674-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Presolol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>56475</Austr>
				<PresentationName>Presolol</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Labetalol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Presolol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcpreso11019</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>labetalol hydrochloride</ActiveIngredient>
						<ReleaseDate>2019-10-30 07:24:03.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>LL 100</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>56475-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>56476</Austr>
				<PresentationName>Presolol</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Labetalol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Presolol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcpreso11019</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>labetalol hydrochloride</ActiveIngredient>
						<ReleaseDate>2019-10-30 07:24:03.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>LL 200</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>56476-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Prexaton</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>119661</Austr>
				<PresentationName>Prexaton</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Bupropion hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>GX CH7</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>119661-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Prexum</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>194884</Austr>
				<PresentationName>Prexum</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Perindopril arginine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Prexum</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>secprexu10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>perindopril</ActiveIngredient>
						<ReleaseDate>2022-07-15 10:50:14.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/07/2014 13:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>194884-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>194885</Austr>
				<PresentationName>Prexum</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Perindopril arginine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Prexum</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>secprexu10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>perindopril</ActiveIngredient>
						<ReleaseDate>2022-07-15 10:50:14.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/07/2014 13:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light green</Colour>
							<Scoring>scored</Scoring>
							<Shape>rod-shaped</Shape>
							<Side1Marking>Servier logo</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>194885-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>194886</Austr>
				<PresentationName>Prexum</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Perindopril arginine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Prexum</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>secprexu10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>perindopril</ActiveIngredient>
						<ReleaseDate>2022-07-15 10:50:14.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/07/2014 13:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>heart</Side1Marking>
							<Side2Marking>Servier logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>194886-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Prexum Combi</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>194917</Austr>
				<PresentationName>Prexum Combi</PresentationName>
    			<PresentionStrength>5mg/1.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Indapamide hemihydrate,Perindopril arginine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Prexum Combi</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>secprexc10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>perindopril with indapamide hemihydrate</ActiveIngredient>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/07/2014 13:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>rod-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>194917-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>279405</Austr>
				<PresentationName>Prexum Combi LD</PresentationName>
    			<PresentionStrength>2.5mg/0.625mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>indapamide hemihydrate,perindopril arginine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Prexum Combi</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>secprexc10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>perindopril with indapamide hemihydrate</ActiveIngredient>
						<ReleaseDate>2022-07-20 16:30:07.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/04/2017 08:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>rod-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>279405-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Prezista</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>153628</Austr>
				<PresentationName>Prezista</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Prezista</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jccprezi11121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>darunavir ethanolate</ActiveIngredient>
						<ReleaseDate>2021-11-17 13:13:24.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/12/2011 10:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>TMC</Side1Marking>
							<Side2Marking>600MG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153628-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Prilace</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>121854</Austr>
				<PresentationName>Prilace</PresentationName>
    			<PresentionStrength>1.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>RP 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121854-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121855</Austr>
				<PresentationName>Prilace</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>RP 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121855-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121856</Austr>
				<PresentationName>Prilace</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>RP 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121856-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>133085</Austr>
				<PresentationName>Prilace</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and blue opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Arrow logo</Side1Marking>
							<Side2Marking>RP 10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133085-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Priligy</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>147946</Austr>
				<PresentationName>Priligy</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>dapoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Priligy tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>dapoxetine hydrochloride</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/09/2018 08:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light grey</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>30 triangle</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>147946-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Primacin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>226430</Austr>
				<PresentationName>Primacin</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablet</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Primaquine phosphate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Primacin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>primaquine phosphate</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2019 14:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>226430-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Primolut</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>134491</Austr>
				<PresentationName>Primolut N</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/09/2014 14:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AN hexagon</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>134491-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Prinivil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>34377</Austr>
				<PresentationName>Prinivil</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lisinopril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 15:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>shield-shaped</Shape>
							<Side1Marking>PRINIVIL</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>34377-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pristiq</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>170674</Austr>
				<PresentationName>Pristiq</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Desvenlafaxine succinate monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Pristiq</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcprist10922</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>desvenlafaxine succinate</ActiveIngredient>
						<ReleaseDate>2022-10-06 09:07:22.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/05/2011 17:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>square pyramid</Shape>
							<Side1Marking>W 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>170674-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>170696</Austr>
				<PresentationName>Pristiq</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Desvenlafaxine succinate monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Pristiq</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>desvenlafaxine succinate</ActiveIngredient>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>30/05/2011 17:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish-orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>square pyramid</Shape>
							<Side1Marking>W 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>170696-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pritor/Amlodipine</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>202106</Austr>
				<PresentationName>Pritor/Amlodipine</PresentationName>
    			<PresentionStrength>40mg/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>amlodipine besilate,telmisartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Pritor/Amlodipine</DocumentName>
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							<DocumentType>eCMI</DocumentType>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>telmisartan with amlodipine besilate</ActiveIngredient>
						<ReleaseDate>2022-07-21 11:06:29.0</ReleaseDate>
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    			<PresentationForm>Tablets</PresentationForm>
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			<brandname>Pro-Banthine</brandname>
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    			<PresentationForm>Tablets</PresentationForm>
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			<brandname>Pro-Cid</brandname>
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				<Austr>74598</Austr>
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			<Presentations>
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    			<PresentationForm>Suppositories</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient>hydrocortisone,cinchocaine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Proctosedyl</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcproct11221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>hydrocortisone with cinchocaine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-02-09 15:22:36.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2010 14:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Suppositories</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>22614-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Procur</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>101531</Austr>
				<PresentationName>Procur</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 13:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101531-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101532</Austr>
				<PresentationName>Procur</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 13:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101532-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Prodeine</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>200605</Austr>
				<PresentationName>Prodeine</PresentationName>
    			<PresentionStrength>500mg/9.6mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>codeine phosphate hemihydrate,Paracetamol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Prodeine</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcproei11221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>codeine phosphate hemihydrate with paracetamol</ActiveIngredient>
						<ReleaseDate>2021-12-08 21:54:28.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/09/2013 14:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>200605-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>205550</Austr>
				<PresentationName>Prodeinextra</PresentationName>
    			<PresentionStrength>500mg/15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>codeine phosphate hemihydrate,Paracetamol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Prodeinextra</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcproex11221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>codeine phosphate hemihydrate with paracetamol</ActiveIngredient>
						<ReleaseDate>2021-12-08 21:50:25.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/09/2013 14:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>PRO 15</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>205550-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>93865</Austr>
				<PresentationName>Prodeine Forte</PresentationName>
    			<PresentionStrength>500mg/30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Paracetamol,Codeine phosphate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Prodeine Forte</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>codeine phosphate hemihydrate with paracetamol</ActiveIngredient>
						<ReleaseDate>2021-12-08 16:59:10.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>P F</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>93865-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Progout</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>17708</Austr>
				<PresentationName>Progout</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Allopurinol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Progout</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>allopurinol</ActiveIngredient>
						<ReleaseDate>2021-09-24 07:51:36.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AL 300</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>17708-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>27969</Austr>
				<PresentationName>Progout</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Allopurinol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Progout</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcprogo20921</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>allopurinol</ActiveIngredient>
						<ReleaseDate>2021-09-24 07:51:36.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AL 100</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>27969-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Prograf</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>158439</Austr>
				<PresentationName>Prograf XL</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tacrolimus</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/11/2010 08:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>XL Capsules</DoseForm>
							<Colour>light yellow and orange</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>0.5mg</Side1Marking>
							<Side2Marking>(Logo) 647</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158439-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158440</Austr>
				<PresentationName>Prograf XL</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tacrolimus</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/11/2010 08:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>XL Capsules</DoseForm>
							<Colour>white and orange</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>1mg</Side1Marking>
							<Side2Marking>(Logo) 677</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158440-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158444</Austr>
				<PresentationName>Prograf XL</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tacrolimus</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/11/2010 08:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>XL Capsules</DoseForm>
							<Colour>greyish red and orange</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>5mg</Side1Marking>
							<Side2Marking>(Logo) 687</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158444-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>58930</Austr>
				<PresentationName>Prograf</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tacrolimus</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Prograf and Advagraf XL</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tacrolimus</ActiveIngredient>
						<ReleaseDate>2022-11-14 16:06:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/07/2008 08:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>1mg</Side1Marking>
							<Side2Marking>[f] 617</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>58930-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>58931</Austr>
				<PresentationName>Prograf</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tacrolimus</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Prograf and Advagraf XL</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tacrolimus</ActiveIngredient>
						<ReleaseDate>2022-11-14 16:06:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/07/2008 08:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>greyish-red</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>5mg</Side1Marking>
							<Side2Marking>[f] 657</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>58931-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>77280</Austr>
				<PresentationName>Prograf</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tacrolimus</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Prograf and Advagraf XL</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>axcprogr11122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tacrolimus</ActiveIngredient>
						<ReleaseDate>2022-11-14 16:06:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/07/2008 08:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>0.5mg</Side1Marking>
							<Side2Marking>[f] 607</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>77280-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Progynova</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10708</Austr>
				<PresentationName>Progynova</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/10/2010 11:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10708-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>10709</Austr>
				<PresentationName>Progynova</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2010 10:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10709-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Proladone</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>14965</Austr>
				<PresentationName>Proladone</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Suppositories</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/01/2010 15:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Suppositories</DoseForm>
							<Colour>off-white</Colour>
							<Scoring></Scoring>
							<Shape>oval/cone-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>14965-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Propecia</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>62084</Austr>
				<PresentationName>Propecia</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Finasteride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Propecia</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcprope10121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>finasteride</ActiveIngredient>
						<ReleaseDate>2021-04-29 09:24:00.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/10/2008 12:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>tan</Colour>
							<Scoring>unscored</Scoring>
							<Shape>octagon-shaped</Shape>
							<Side1Marking>PROPECIA</Side1Marking>
							<Side2Marking>P logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62084-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Propranolol (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>222958</Austr>
				<PresentationName>APO-Propranolol</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Propranolol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>P 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>222958-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>222969</Austr>
				<PresentationName>APO-Propranolol</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Propranolol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>P 40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>222969-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Proscar</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>43667</Austr>
				<PresentationName>Proscar</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Finasteride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Proscar</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcprosc10121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>finasteride</ActiveIngredient>
						<ReleaseDate>2021-04-29 13:19:42.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/10/2008 12:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>apple-shaped</Shape>
							<Side1Marking>PROSCAR</Side1Marking>
							<Side2Marking>MSD 72</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>43667-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Provera</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>12331</Austr>
				<PresentationName>Provera</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Medroxyprogesterone acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Provera</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcprovt10420</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>medroxyprogesterone acetate</ActiveIngredient>
						<ReleaseDate>2020-05-12 15:44:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/09/2008 14:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>U 467</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>12331-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>12333</Austr>
				<PresentationName>Provera</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Medroxyprogesterone acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Provera</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcprovt10420</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>medroxyprogesterone acetate</ActiveIngredient>
						<ReleaseDate>2020-05-12 15:44:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/09/2008 14:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>U 320</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>12333-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>12334</Austr>
				<PresentationName>Provera</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Medroxyprogesterone acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Provera</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcprovt10420</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>medroxyprogesterone acetate</ActiveIngredient>
						<ReleaseDate>2020-05-12 15:44:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/09/2008 14:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>U 403</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>12334-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>12336</Austr>
				<PresentationName>Provera</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Medroxyprogesterone acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Provera</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcprovt10420</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>medroxyprogesterone acetate</ActiveIngredient>
						<ReleaseDate>2020-05-12 15:44:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/09/2008 14:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>UPJOHN 717</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>12336-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>42932</Austr>
				<PresentationName>Provera</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Medroxyprogesterone acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Provera</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcprovt10420</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>medroxyprogesterone acetate</ActiveIngredient>
						<ReleaseDate>2020-05-12 15:44:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/09/2008 14:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>U 64</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>42932-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>42933</Austr>
				<PresentationName>Provera</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Medroxyprogesterone acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Provera</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcprovt10420</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>medroxyprogesterone acetate</ActiveIngredient>
						<ReleaseDate>2020-05-12 15:44:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/09/2008 14:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>286 286</Side1Marking>
							<Side2Marking>U</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>42933-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>42934</Austr>
				<PresentationName>Provera</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Medroxyprogesterone acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Provera</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcprovt10420</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>medroxyprogesterone acetate</ActiveIngredient>
						<ReleaseDate>2020-05-12 15:44:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/09/2008 14:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>UPJOHN 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>42934-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>42935</Austr>
				<PresentationName>Provera</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Medroxyprogesterone acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Provera</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcprovt10420</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>medroxyprogesterone acetate</ActiveIngredient>
						<ReleaseDate>2020-05-12 15:44:12.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/09/2008 13:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>UPJOHN 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>42935-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Proviron</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>136196</Austr>
				<PresentationName>Proviron</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/09/2014 14:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AX hexagon</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>136196-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Proxen</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>259112</Austr>
				<PresentationName>Proxen SR</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Naproxen</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Proxen SR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>iycproxs10821</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>naproxen</ActiveIngredient>
						<ReleaseDate>2021-08-31 16:39:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/01/2017 16:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>NPR SR-1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>259112-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>259113</Austr>
				<PresentationName>Proxen SR</PresentationName>
    			<PresentionStrength>750mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Naproxen</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Proxen SR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>iycproxs10821</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>naproxen</ActiveIngredient>
						<ReleaseDate>2021-08-31 16:39:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/01/2017 17:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>NPR SR-750</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>259113-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>47373</Austr>
				<PresentationName>Proxen SR</PresentationName>
    			<PresentionStrength>750mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Naproxen</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/09/2008 16:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>NPR SR-750</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>47373-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>47442</Austr>
				<PresentationName>Proxen SR</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Naproxen</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/09/2008 16:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>NPR SR-1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>47442-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Prozac</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>14653</Austr>
				<PresentationName>Prozac</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Prozac</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>lycprozc11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fluoxetine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-14 17:02:43.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/02/2009 09:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green and off-white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Lilly 3105</Side1Marking>
							<Side2Marking>Lilly 3105</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>14653-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>61081</Austr>
				<PresentationName>Prozac</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/02/2009 09:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>4400</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>61081-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pryzex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>178975</Austr>
				<PresentationName>Pryzex</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/10/2018 16:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>178975-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>178987</Austr>
				<PresentationName>Pryzex</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/10/2018 16:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>178987-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>178991</Austr>
				<PresentationName>Pryzex</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/10/2018 16:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>178991-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>178996</Austr>
				<PresentationName>Pryzex</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/10/2018 16:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>178996-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179071</Austr>
				<PresentationName>Pryzex ODT</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/07/2019 16:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179071-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179076</Austr>
				<PresentationName>Pryzex ODT</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/04/2018 15:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179076-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179079</Austr>
				<PresentationName>Pryzex ODT</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/04/2018 13:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179079-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179082</Austr>
				<PresentationName>Pryzex ODT</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/07/2019 16:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179082-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pseudoephedrine (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>191938</Austr>
				<PresentationName>Pharmacy Action Sinus &amp; Nasal Decongestant Relief</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/10/2012 12:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>191938-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>PTU</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>13319</Austr>
				<PresentationName>PTU</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/01/2010 15:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PRESTAB</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>13319-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Puri-Nethol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10993</Austr>
				<PresentationName>Puri-Nethol</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Mercaptopurine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/10/2010 08:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>GX EX2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10993-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pyralin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>58398</Austr>
				<PresentationName>Pyralin EN</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Sulfasalazine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Pyralin EN</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcpyrat10919</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>sulfasalazine</ActiveIngredient>
						<ReleaseDate>2019-09-17 15:39:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/07/2013 14:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow-orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>KPh</Side1Marking>
							<Side2Marking>102</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>58398-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Pyroxin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>27527</Austr>
				<PresentationName>Pyroxin</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>27527-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Qlaira</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>149319</Austr>
				<PresentationName>Qlaira</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/11/2014 12:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DD hexagon</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>149319-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>medium red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DJ hexagon</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>149319-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>3</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DH hexagon</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>149319-C03-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>4</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DN hexagon</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>149319-C04-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>5</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DT hexagon</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>149319-C05-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Qpril</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>96915</Austr>
				<PresentationName>Qpril</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Quinapril hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Qpril</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcqpril21119</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>quinapril hydrochloride</ActiveIngredient>
						<ReleaseDate>2019-11-25 09:06:15.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/10/2010 16:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>QP 5</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96915-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>96923</Austr>
				<PresentationName>Qpril</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Quinapril hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Qpril</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcqpril21119</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>quinapril hydrochloride</ActiveIngredient>
						<ReleaseDate>2019-11-25 09:06:15.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/10/2010 16:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>QP 10</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96923-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>96924</Austr>
				<PresentationName>Qpril</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Quinapril hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Qpril</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcqpril21119</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>quinapril hydrochloride</ActiveIngredient>
						<ReleaseDate>2019-11-25 09:06:15.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>21/10/2010 16:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>QP 20</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96924-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Qtern</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>255632</Austr>
				<PresentationName>Qtern</PresentationName>
    			<PresentionStrength>5mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Saxagliptin,Dapagliflozin propanediol monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>QTERN</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apcqtern10922</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>saxagliptin with dapagliflozin</ActiveIngredient>
						<ReleaseDate>2022-09-19 11:15:07.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/12/2018 08:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light brown to brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>1122</Side1Marking>
							<Side2Marking>5/10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>255632-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quetia</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>204153</Austr>
				<PresentationName>Quetia</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204153-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>204154</Austr>
				<PresentationName>Quetia</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204154-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>204155</Austr>
				<PresentationName>Quetia</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>204155-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>204155-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>204156</Austr>
				<PresentationName>Quetia</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204156-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quetia XR</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>199872</Austr>
				<PresentationName>Quetia XR</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/07/2021 16:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199872-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199874</Austr>
				<PresentationName>Quetia XR</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/07/2021 16:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199874-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199878</Austr>
				<PresentationName>Quetia XR</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2022 09:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink to pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199878-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199886</Austr>
				<PresentationName>Quetia XR</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/04/2018 13:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199886-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199889</Austr>
				<PresentationName>Quetia XR</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/07/2021 16:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199889-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quetiapine (Actavis)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>179898</Austr>
				<PresentationName>Quetiapine Actavis</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 14:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Q</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179898-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179899</Austr>
				<PresentationName>Quetiapine Actavis</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 14:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>Q</Side1Marking>
							<Side2Marking>300</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179899-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179900</Austr>
				<PresentationName>Quetiapine Actavis</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 14:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>Q</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179900-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179904</Austr>
				<PresentationName>Quetiapine Actavis</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 15:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Q</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179904-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quetiapine (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>170851</Austr>
				<PresentationName>Quetiapine AN</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/10/2017 13:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>170851-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>170853</Austr>
				<PresentationName>Quetiapine AN</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/10/2017 13:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>170853-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>170854</Austr>
				<PresentationName>Quetiapine AN</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/10/2017 13:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>170854-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>170854-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>170856</Austr>
				<PresentationName>Quetiapine AN</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/10/2017 13:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>170856-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>172838</Austr>
				<PresentationName>Quetiapine CH</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/08/2012 13:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>E 53</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>172838-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>172841</Austr>
				<PresentationName>Quetiapine CH</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/08/2012 13:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>E 52</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>172841-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>172848</Austr>
				<PresentationName>Quetiapine CH</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/08/2012 13:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>E 56</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>172848-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>172858</Austr>
				<PresentationName>Quetiapine CH</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/08/2012 13:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>E 55</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>172858-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quetiapine (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>166059</Austr>
				<PresentationName>APO-Quetiapine</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/07/2012 13:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>QUE 300</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166059-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166064</Austr>
				<PresentationName>APO-Quetiapine</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/07/2012 13:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>QUE 200</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166064-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166077</Austr>
				<PresentationName>APO-Quetiapine</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/07/2012 13:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>QUE 100</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166077-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166082</Austr>
				<PresentationName>APO-Quetiapine</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/07/2012 13:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>QUE 25</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166082-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>204157</Austr>
				<PresentationName>Quetiapine Apotex</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/04/2020 09:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204157-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>204158</Austr>
				<PresentationName>Quetiapine Apotex</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2022 10:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204158-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>204159</Austr>
				<PresentationName>Quetiapine Apotex</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2022 10:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>204159-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>204159-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>204160</Austr>
				<PresentationName>Quetiapine Apotex</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2022 10:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204160-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>226800</Austr>
				<PresentationName>APO-Quetiapine XR</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/12/2016 10:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>I4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>226800-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>226800-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>226818</Austr>
				<PresentationName>APO-Quetiapine XR</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/12/2016 10:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Q 300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>226818-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>226821</Austr>
				<PresentationName>APO-Quetiapine XR</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/12/2016 10:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>I2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>226821-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>241755</Austr>
				<PresentationName>APO-Quetiapine XR</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/12/2016 10:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Q 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>241755-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quetiapine (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>166065</Austr>
				<PresentationName>Chemmart Quetiapine </PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/07/2012 14:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>QUE 25</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166065-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166067</Austr>
				<PresentationName>Chemmart Quetiapine</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/07/2012 14:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>QUE 200</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166067-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166068</Austr>
				<PresentationName>Chemmart Quetiapine</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/07/2012 14:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>QUE 300</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166068-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166079</Austr>
				<PresentationName>Chemmart Quetiapine</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/07/2012 14:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>QUE 100</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166079-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quetiapine (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>176710</Austr>
				<PresentationName>Quetiapine-GA</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 12:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Q</Side1Marking>
							<Side2Marking>25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>176710-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>176718</Austr>
				<PresentationName>Quetiapine-GA</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 14:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>Q</Side1Marking>
							<Side2Marking>300</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>176718-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>176719</Austr>
				<PresentationName>Quetiapine-GA</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 12:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Q</Side1Marking>
							<Side2Marking>200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>176719-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quetiapine (Generic Health)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>179895</Austr>
				<PresentationName>Quetiapine GH</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Q</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179895-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179896</Austr>
				<PresentationName>Quetiapine GH</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>Q</Side1Marking>
							<Side2Marking>300</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179896-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179897</Austr>
				<PresentationName>Quetiapine GH</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>Q</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179897-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179902</Austr>
				<PresentationName>Quetiapine GH</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Q</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179902-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quetiapine (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>204819</Austr>
				<PresentationName>Pharmacor Quetiapine</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/07/2014 15:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>260</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204819-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>204824</Austr>
				<PresentationName>Pharmacor Quetiapine</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/07/2014 15:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>259</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204824-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>204829</Austr>
				<PresentationName>Pharmacor Quetiapine</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/07/2014 15:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>261</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204829-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>204843</Austr>
				<PresentationName>Pharmacor Quetiapine</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/07/2014 15:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>262</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204843-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quetiapine (Ranbaxy)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>166420</Austr>
				<PresentationName>Quetiapine RBX</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>Q6</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166420-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166429</Austr>
				<PresentationName>Quetiapine RBX</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Q3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166429-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166434</Austr>
				<PresentationName>Quetiapine RBX</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Q1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166434-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166435</Austr>
				<PresentationName>Quetiapine RBX</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Q5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166435-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quetiapine (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>158099</Austr>
				<PresentationName>Quetiapine Sandoz</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 12:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>158099-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>158099-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158104</Austr>
				<PresentationName>Quetiapine Sandoz</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 13:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158104-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158106</Austr>
				<PresentationName>Quetiapine Sandoz</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 13:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158106-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158109</Austr>
				<PresentationName>Quetiapine Sandoz</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 13:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158109-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quetiapine (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>166060</Austr>
				<PresentationName>Terry White Chemists Quetiapine</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/09/2012 16:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>QUE 25</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166060-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166066</Austr>
				<PresentationName>Terry White Chemists Quetiapine</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/09/2012 16:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>QUE 100</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166066-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166069</Austr>
				<PresentationName>Terry White Chemists Quetiapine</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/09/2012 16:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>QUE 300</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166069-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166076</Austr>
				<PresentationName>Terry White Chemists Quetiapine</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/09/2012 16:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>QUE 200</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166076-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quetiapine-AS XR</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>226819</Austr>
				<PresentationName>Quetiapine-AS XR</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/04/2018 13:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>I4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>226819-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>226819-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>226820</Austr>
				<PresentationName>Quetiapine-AS XR</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/04/2018 13:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>I2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>226820-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>241756</Austr>
				<PresentationName>Quetiapine-AS XR</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/04/2018 13:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Q 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>241756-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quilonum</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>53377</Austr>
				<PresentationName>Quilonum SR</PresentationName>
    			<PresentionStrength>450mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lithium carbonate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 15:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>53377-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quinapril (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>133220</Austr>
				<PresentationName>Apo-Quinapril</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quinapril hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/06/2011 10:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133220-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>133221</Austr>
				<PresentationName>Apo-Quinapril</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quinapril hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>13/08/2008 13:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133221-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quinapril (Arrow)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>118750</Austr>
				<PresentationName>Quinapril Arrow</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 08:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>118750-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>118751</Austr>
				<PresentationName>Quinapril Arrow</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to almost white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>118751-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>118752</Austr>
				<PresentationName>Quinapril Arrow</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 08:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>118752-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quinapril (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>133233</Austr>
				<PresentationName>Quinapril-GA</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 13:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133233-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>133234</Austr>
				<PresentationName>Quinapril-GA</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 13:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133234-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>133235</Austr>
				<PresentationName>Quinapril-GA</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 13:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133235-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quinapril (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>133201</Austr>
				<PresentationName>Quinapril generichealth</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/12/2008 14:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133201-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quinapril (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>117218</Austr>
				<PresentationName>Quinapril Sandoz</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quinapril hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 11:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>QP 5</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>117218-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>117226</Austr>
				<PresentationName>Quinapril Sandoz</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quinapril hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/02/2010 10:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>QP 20</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>117226-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quinapril hydrochloride (Pfizer)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>123434</Austr>
				<PresentationName>Quinapril Pfizer</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quinapril hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish-brown</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking>5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>123434-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>123435</Austr>
				<PresentationName>Quinapril Pfizer</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quinapril hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish-brown</Colour>
							<Scoring>scored</Scoring>
							<Shape>triangular</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>123435-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>123436</Austr>
				<PresentationName>Quinapril Pfizer</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quinapril hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish-brown</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>123436-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quinate</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>50707</Austr>
				<PresentationName>Quinate</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Quinine sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/11/2008 13:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>50707-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quinbisul</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>116545</Austr>
				<PresentationName>Quinbisul</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Quinine bisulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>116545-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Quipine</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>162385</Austr>
				<PresentationName>Quipine</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/06/2012 08:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>QTP</Side1Marking>
							<Side2Marking>25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>162385-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>162386</Austr>
				<PresentationName>Quipine</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/06/2012 08:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>QTP</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>162386-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>162388</Austr>
				<PresentationName>Quipine</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/06/2012 08:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>QTP</Side1Marking>
							<Side2Marking>200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>162388-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>162388-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>162389</Austr>
				<PresentationName>Quipine</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/06/2012 08:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>QTP</Side1Marking>
							<Side2Marking>300</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>162389-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rabeprazole sodium (Actavis)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>191860</Austr>
				<PresentationName>Rabeprazole Actavis</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 15:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>191860-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rabeprazole sodium (Amneal)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>189244</Austr>
				<PresentationName>Rabeprazole AN</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rabeprazole sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/10/2017 13:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>189244-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rabeprazole sodium (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>245232</Austr>
				<PresentationName>APO-Rabeprazole</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rabeprazole sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/12/2016 10:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>245232-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>245233</Austr>
				<PresentationName>APO-Rabeprazole</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rabeprazole sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>08/12/2016 10:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>245233-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rabeprazole sodium (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>211969</Austr>
				<PresentationName>Chemmart Rabeprazole</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rabeprazole sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/08/2015 12:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>211969-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>245234</Austr>
				<PresentationName>Chemmart Rabeprazole </PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rabeprazole sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/05/2017 11:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>245234-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>245235</Austr>
				<PresentationName>Chemmart Rabeprazole </PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rabeprazole sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/05/2017 11:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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								<ImageFileName>245235-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rabeprazole sodium (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>189747</Austr>
				<PresentationName>Rabeprazole generichealth</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>189748</Austr>
				<PresentationName>Rabeprazole generichealth</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>23/06/2015 15:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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								<ImageFileName>189748-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rabeprazole sodium (Mylan)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>189755</Austr>
				<PresentationName>Rabeprazole Mylan</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Rabeprazole Mylan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcrabem10121</Filename>
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						<ActiveIngredient>rabeprazole sodium</ActiveIngredient>
						<ReleaseDate>2021-01-22 10:50:54.0</ReleaseDate>
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				<Images>
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						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/03/2022 12:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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			</Presentations>
		</Brand><Brand>
			<brandname>Rabeprazole sodium (Sandoz)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>173080</Austr>
				<PresentationName>Rabeprazole Sandoz</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rabeprazole sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<VersionStatus>Current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
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							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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				</Images>
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			<Presentations>
				<Austr>173081</Austr>
				<PresentationName>Rabeprazole Sandoz</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rabeprazole sodium</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rabeprazole sodium (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>211971</Austr>
				<PresentationName>Terry White Chemists Rabeprazole</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rabeprazole sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Austr>175231</Austr>
				<PresentationName>Ramipril AN</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
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						<DateEffective>13/10/2017 13:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink mottled</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>H 19</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>175231-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>175233</Austr>
				<PresentationName>Ramipril AN</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/10/2017 13:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>H 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>175233-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>175239</Austr>
				<PresentationName>Ramipril AN</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
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						<DateEffective>13/10/2017 13:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow to yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>H 18</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>175239-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>203711</Austr>
				<PresentationName>Ramipril AN</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/06/2019 09:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>D</Side1Marking>
							<Side2Marking>43</Side2Marking>
							<Views>
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								<ViewLabel>C</ViewLabel>
								<ImageFileName>203711-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ramipril (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>179026</Austr>
				<PresentationName>APO-Ramipril Capsules</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 13:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>2.5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179026-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179028</Austr>
				<PresentationName>APO-Ramipril Capsules</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 13:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179028-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179033</Austr>
				<PresentationName>APO-Ramipril Capsules</PresentationName>
    			<PresentionStrength>1.25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 13:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>1.25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179033-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179034</Austr>
				<PresentationName>APO-Ramipril Capsules</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/03/2013 13:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>APO</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179034-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>231161</Austr>
				<PresentationName>APO-Ramipril Tablets</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink to red mottled</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>R 18</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>231161-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>231162</Austr>
				<PresentationName>APO-Ramipril Tablets</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/04/2020 09:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow to yellow mottled</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>R 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>231162-C01-02-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>231163</Austr>
				<PresentationName>APO-Ramipril Tablets</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>22/05/2016 20:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow to yellow mottled</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>R 19</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>231163-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Ramipril (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>134788</Austr>
				<PresentationName>Ramipril-GA</PresentationName>
    			<PresentionStrength>1.25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>14/12/2009 13:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>RAMI</Side1Marking>
							<Side2Marking>1.25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>134788-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>134793</Austr>
				<PresentationName>Ramipril-GA</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/12/2009 13:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>RAMI</Side1Marking>
							<Side2Marking>2.5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>134793-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>134798</Austr>
				<PresentationName>Ramipril-GA</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/12/2009 13:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>RAMI</Side1Marking>
							<Side2Marking>5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>134798-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>134803</Austr>
				<PresentationName>Ramipril-GA</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/12/2009 13:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>RAMI</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>134803-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ramipril (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>134792</Austr>
				<PresentationName>Ramipril generichealth</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/11/2008 17:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>RAMI</Side1Marking>
							<Side2Marking>2.5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>134792-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>134797</Austr>
				<PresentationName>Ramipril generichealth</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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			<Presentations>
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			<Presentations>
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			<Presentations>
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			<Presentations>
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			<Presentations>
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			<Presentations>
				<Austr>285693</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>191837</Austr>
				<PresentationName>Pharmacy Action Heartburn &amp; Acid Indigestion Relief</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>creamish yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>R 150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>191837-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>191838</Austr>
				<PresentationName>Pharmacy Action Heartburn &amp; Acid Indigestion Relief Forte</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>creamish yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>R 300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>191838-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>191838-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>219141</Austr>
				<PresentationName>Ranitidine GH</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/05/2017 17:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>219141-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>219142</Austr>
				<PresentationName>Ranitidine GH</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/05/2017 17:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>219142-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ranitidine (GenRx)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>121977</Austr>
				<PresentationName>GenRx Ranitidine</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ranitidine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/06/2013 11:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RAN 150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121977-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121980</Austr>
				<PresentationName>GenRx Ranitidine</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ranitidine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/06/2013 11:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>RAN 300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121980-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ranitidine (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>70325</Austr>
				<PresentationName>Ranitidine Sandoz</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ranitidine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 13:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>70325-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>70356</Austr>
				<PresentationName>Ranitidine Sandoz</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ranitidine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 13:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>70356-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ranitidine (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>121975</Austr>
				<PresentationName>Terry White Chemists Ranitidine</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ranitidine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/06/2013 11:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RAN 150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121975-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>121978</Austr>
				<PresentationName>Terry White Chemists Ranitidine</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ranitidine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/06/2013 11:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>RAN 300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121978-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ranitidine-WT</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>82324</Austr>
				<PresentationName>Ranitidine-WT</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 13:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>creamish-yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RAN 150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82324-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ransim</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>120591</Austr>
				<PresentationName>Ransim</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 10:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SST</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>120591-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>120612</Austr>
				<PresentationName>Ransim</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 10:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>tan</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SST</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>120612-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>120616</Austr>
				<PresentationName>Ransim</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 10:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brick-red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SST</Side1Marking>
							<Side2Marking>40</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>120616-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>120617</Austr>
				<PresentationName>Ransim</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 10:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brick-red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RX 793</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>120617-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>120617-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ranzepam</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>134473</Austr>
				<PresentationName>Ranzepam</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 10:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>134473-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
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			<Presentations>
				<Austr>134589</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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			</Presentations>
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			<Presentations>
				<Austr>125629</Austr>
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    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			</Presentations>
			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DocumentName>Rapamune Tablets</DocumentName>
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			</Presentations>
			<Presentations>
				<Austr>169305</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<brandname>Rasagiline Mesilate (Teva)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>294880</Austr>
				<PresentationName>Rasagiline-Teva</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Rasagiline-Teva</DocumentName>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
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							<Side1Marking>GIL 1</Side1Marking>
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							<Views>
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			</Presentations>
		</Brand><Brand>
			<brandname>Rasalect</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>319000</Austr>
				<PresentationName>Rasalect</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DocumentName>Rasalect</DocumentName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Reaptan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>170796</Austr>
				<PresentationName>Reaptan</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Perindopril arginine,Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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							<View>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>170797</Austr>
				<PresentationName>Reaptan</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Amlodipine besylate,Perindopril arginine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Reaptan</DocumentName>
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							<Side1Marking>5/10</Side1Marking>
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							<Views>
							<View>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>170798</Austr>
				<PresentationName>Reaptan</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Amlodipine besylate,Perindopril arginine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Reaptan</DocumentName>
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				<Images>
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							<Views>
							<View>
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							</Views>
						</Phase>
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			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Perindopril arginine,Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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			<brandname>Retrovir</brandname>
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			<Presentations>
				<Austr>10969</Austr>
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    			<PresentationForm>Capsules</PresentationForm>
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    			<Container>bottle</Container>
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			<Presentations>
				<Austr>10996</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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							<Shape></Shape>
							<Side1Marking>Unicorn logo Wellcome</Side1Marking>
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			<Presentations>
				<Austr>178383</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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			<Presentations>
				<Austr>119102</Austr>
				<PresentationName>Revatio</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
				<Austr>159973</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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		</Brand><Brand>
			<brandname>Risperdal</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>47008</Austr>
				<PresentationName>Risperdal Tablets</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
				<Austr>47010</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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						<DocumentName>Risperdal Tablets and Solution</DocumentName>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
				<Austr>48486</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DocumentName>Risperdal Tablets and Solution</DocumentName>
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			</Presentations>
			<Presentations>
				<Austr>71849</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
				<Austr>159969</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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							<Views>
							<View>
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				<Austr>159972</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
				<Austr>159975</Austr>
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    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/05/2013 16:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159975-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>159978</Austr>
				<PresentationName>Rispericor</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/05/2013 16:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159978-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>159979</Austr>
				<PresentationName>Rispericor</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/05/2013 16:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brick red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159979-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Risperidone (Actavis)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>159976</Austr>
				<PresentationName>Risperidone Actavis</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 15:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159976-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Risperidone (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>166680</Austr>
				<PresentationName>Risperidone AN</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/06/2012 14:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>5 2</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166680-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166681</Austr>
				<PresentationName>Risperidone AN</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/06/2012 14:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>5 1</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166681-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166682</Austr>
				<PresentationName>Risperidone AN</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/06/2012 14:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>5 0</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166682-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166683</Austr>
				<PresentationName>Risperidone AN</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/06/2012 11:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>5 3</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166683-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166685</Austr>
				<PresentationName>Risperidone AN</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/06/2012 14:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>5 4</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166685-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Risperidone (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>127606</Austr>
				<PresentationName>APO-Risperidone</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/06/2009 09:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brownish-red</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>RI .5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127606-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127608</Austr>
				<PresentationName>APO-Risperidone</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/06/2009 09:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>RI 1</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127608-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127610</Austr>
				<PresentationName>APO-Risperidone</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/06/2009 09:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>RI 2</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127610-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127612</Austr>
				<PresentationName>APO-Risperidone</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/06/2009 09:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>RI 3</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127612-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127615</Austr>
				<PresentationName>APO-Risperidone</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-22 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/06/2009 09:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light green</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>RI 4</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127615-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>304250</Austr>
				<PresentationName>APO-Risperidone</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/04/2020 09:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brick red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>304250-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>304251</Austr>
				<PresentationName>APO-Risperidone </PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/03/2020 20:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>304251-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>304252</Austr>
				<PresentationName>APO-Risperidone</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/03/2020 20:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>304252-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>304253</Austr>
				<PresentationName>APO-Risperidone</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/03/2020 20:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>304253-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>304254</Austr>
				<PresentationName>APO-Risperidone</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/03/2020 20:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>304254-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Risperidone (Arrow)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>127880</Austr>
				<PresentationName>Risperidone ARW</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>R</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127880-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127882</Austr>
				<PresentationName>Risperidone ARW</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>R 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127882-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127884</Austr>
				<PresentationName>Risperidone ARW</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>R 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127884-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127886</Austr>
				<PresentationName>Risperidone ARW</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>R 3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127886-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127888</Austr>
				<PresentationName>Risperidone ARW</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/07/2018 11:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>R 4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127888-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Risperidone (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>127764</Austr>
				<PresentationName>Risperidone-GA</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 13:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>R</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127764-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127770</Austr>
				<PresentationName>Risperidone-GA</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 13:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>R 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127770-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127779</Austr>
				<PresentationName>Risperidone-GA</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 13:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>R 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127779-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127787</Austr>
				<PresentationName>Risperidone-GA</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 13:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>R 3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127787-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127862</Austr>
				<PresentationName>Risperidone-GA</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 13:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>R 4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127862-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Risperidone (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>139801</Austr>
				<PresentationName>Risperidone generichealth</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/09/2011 15:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>139801-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>139813</Austr>
				<PresentationName>Risperidone generichealth</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>17/06/2010 11:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>139813-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>139821</Austr>
				<PresentationName>Risperidone generichealth</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>17/06/2010 11:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>139821-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>139824</Austr>
				<PresentationName>Risperidone generichealth</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>17/06/2010 11:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red-brown</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>139824-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Risperidone (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>126148</Austr>
				<PresentationName>Risperidone Sandoz</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 13:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>126148-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>126158</Austr>
				<PresentationName>Risperidone Sandoz</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 13:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>apricot</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>126158-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>126159</Austr>
				<PresentationName>Risperidone Sandoz</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 13:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>126159-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>126160</Austr>
				<PresentationName>Risperidone Sandoz</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 13:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>126160-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>147326</Austr>
				<PresentationName>Risperidone Sandoz</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 13:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>147326-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ritalin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>11052</Austr>
				<PresentationName>Ritalin</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Methylphenidate hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Ritalin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcrtlor10422</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>methylphenidate hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-04-13 08:04:29.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/01/2011 13:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AB</Side1Marking>
							<Side2Marking>CG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>11052-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>160228</Austr>
				<PresentationName>Ritalin LA </PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Methylphenidate hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Ritalin LA</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcrtlla10422</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>methylphenidate hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-04-13 08:32:35.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/01/2011 13:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light brown and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>NVR</Side1Marking>
							<Side2Marking>R10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>160228-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>82957</Austr>
				<PresentationName>Ritalin LA</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Methylphenidate hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Ritalin LA</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcrtlla10422</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>methylphenidate hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-04-13 08:32:35.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/04/2009 11:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>NVR</Side1Marking>
							<Side2Marking>R20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82957-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>82958</Austr>
				<PresentationName>Ritalin LA</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Methylphenidate hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Ritalin LA</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcrtlla10422</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>methylphenidate hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-04-13 08:32:35.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/12/2008 12:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>NVR</Side1Marking>
							<Side2Marking>R30</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82958-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>82959</Austr>
				<PresentationName>Ritalin LA</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Methylphenidate hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Ritalin LA</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcrtlla10422</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>methylphenidate hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-04-13 08:32:35.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>22/04/2009 11:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light brown</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>NVR</Side1Marking>
							<Side2Marking>R40</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82959-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rithmik</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>98655</Austr>
				<PresentationName>Rithmik</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amiodarone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>98655-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rivotril</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>13759</Austr>
				<PresentationName>Rivotril</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Clonazepam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/09/2008 16:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROCHE 0.5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>13759-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>285708</Austr>
				<PresentationName>Rivotril</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Clonazepam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/08/2021 16:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROCHE 0.5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>285708-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>42373</Austr>
				<PresentationName>Rivotril</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Clonazepam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/09/2008 16:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROCHE 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>42373-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rixadone</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>199178</Austr>
				<PresentationName>Rixadone</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Risperidone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
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				<Austr>78503</Austr>
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    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Lozenges</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/02/2010 14:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Lozenges</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>R</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>78503-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>78503-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rocaltrol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>92969</Austr>
				<PresentationName>Rocaltrol</PresentationName>
    			<PresentionStrength>0.25mcg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Calcitriol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Rocaltrol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>iycrocal10321</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>calcitriol</ActiveIngredient>
						<ReleaseDate>2021-04-15 16:41:32.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/12/2010 11:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>brown/red-orange and white to grey yellow/orange</Colour>
							<Scoring></Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>92969-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ropinirole (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>189856</Austr>
				<PresentationName>Ropinirole-GA</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 12:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>pentagonal-shaped</Shape>
							<Side1Marking>4891</Side1Marking>
							<Side2Marking>SB</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>189856-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>190143</Austr>
				<PresentationName>Ropinirole-GA</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 12:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellowish pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>pentagonal-shaped</Shape>
							<Side1Marking>4893</Side1Marking>
							<Side2Marking>SB</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>190143-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ropinirole ARW</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>96866</Austr>
				<PresentationName>Ropinirole ARW</PresentationName>
    			<PresentionStrength>0.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ropinirole hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/06/2012 11:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>pentagonal-shaped</Shape>
							<Side1Marking>4890</Side1Marking>
							<Side2Marking>SB</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96866-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>96868</Austr>
				<PresentationName>Ropinirole ARW</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ropinirole hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/06/2012 11:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>pentagonal-shaped</Shape>
							<Side1Marking>4891</Side1Marking>
							<Side2Marking>SB</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96868-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>96870</Austr>
				<PresentationName>Ropinirole ARW</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ropinirole hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/06/2012 11:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellowish pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>pentagonal-shaped</Shape>
							<Side1Marking>4893</Side1Marking>
							<Side2Marking>SB</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96870-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rosuvastatin (Ranbaxy)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>184707</Austr>
				<PresentationName>Rosuvastatin RBX</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink to pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RT 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184707-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>184709</Austr>
				<PresentationName>Rosuvastatin RBX</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow to yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RT 1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184709-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>184717</Austr>
				<PresentationName>Rosuvastatin RBX</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink to pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RT 3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184717-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>184721</Austr>
				<PresentationName>Rosuvastatin RBX</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink to pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>RT 4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>184721-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rosuvastatin (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>183577</Austr>
				<PresentationName>Rosuvastatin Sandoz</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/08/2013 14:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RSV 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183577-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183595</Austr>
				<PresentationName>Rosuvastatin Sandoz</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/08/2013 14:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RSV 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183595-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183597</Austr>
				<PresentationName>Rosuvastatin Sandoz</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/08/2013 14:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RSV 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183597-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183599</Austr>
				<PresentationName>Rosuvastatin Sandoz</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/08/2013 14:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RSV 40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183599-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rosuvastatin calcium (Actavis)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>183634</Austr>
				<PresentationName>Rosuvastatin Actavis</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 12:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ST1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183634-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183639</Austr>
				<PresentationName>Rosuvastatin Actavis</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>25/11/2013 12:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ST2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183639-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183643</Austr>
				<PresentationName>Rosuvastatin Actavis</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 12:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ST3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183643-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183647</Austr>
				<PresentationName>Rosuvastatin Actavis</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 12:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>ST4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183647-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rosuvastatin calcium (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>183057</Austr>
				<PresentationName>APO-Rosuvastatin</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/08/2013 13:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROS 20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183057-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183061</Austr>
				<PresentationName>APO-Rosuvastatin</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/08/2013 13:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROS 5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183061-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183073</Austr>
				<PresentationName>APO-Rosuvastatin</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/08/2013 13:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROS 10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183073-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183074</Austr>
				<PresentationName>APO-Rosuvastatin</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/08/2013 13:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>ROS40</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183074-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>234460</Austr>
				<PresentationName>Rosuvastatin Apotex</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/04/2019 18:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>R</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234460-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>234484</Austr>
				<PresentationName>Rosuvastatin Apotex</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/04/2019 18:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>R</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234484-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rosuvastatin calcium (Arrow)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>234527</Austr>
				<PresentationName>Rosuvastatin ARW</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/03/2018 11:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>R</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234527-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>234528</Austr>
				<PresentationName>Rosuvastatin ARW</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/03/2018 11:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>R</Side1Marking>
							<Side2Marking>5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234528-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rosuvastatin calcium (Blooms the Chemist)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>183056</Austr>
				<PresentationName>Blooms the Chemist Rosuvastatin </PresentationName>
    			<PresentionStrength>20 mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/08/2015 12:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROS 20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183056-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183064</Austr>
				<PresentationName>Blooms the Chemist Rosuvastatin </PresentationName>
    			<PresentionStrength>10 mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/08/2015 12:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROS 10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183064-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183070</Austr>
				<PresentationName>Blooms the Chemist Rosuvastatin </PresentationName>
    			<PresentionStrength>5 mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/08/2015 12:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROS 5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183070-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183072</Austr>
				<PresentationName>Blooms the Chemist Rosuvastatin </PresentationName>
    			<PresentionStrength>40 mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/08/2015 12:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>ROS 40</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183072-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>234483</Austr>
				<PresentationName>BTC Rosuvastatin</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/10/2019 08:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>R</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234483-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>234498</Austr>
				<PresentationName>BTC Rosuvastatin</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/10/2019 08:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>R</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234498-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rosuvastatin calcium (Chemmart)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>183063</Austr>
				<PresentationName>Chemmart Rosuvastatin </PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/08/2013 13:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROS 5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183063-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183066</Austr>
				<PresentationName>Chemmart Rosuvastatin </PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/08/2013 13:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROS 10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183066-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183069</Austr>
				<PresentationName>Chemmart Rosuvastatin </PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/08/2013 13:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>ROS40</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183069-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183071</Austr>
				<PresentationName>Chemmart Rosuvastatin </PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/08/2013 13:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROS 20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183071-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rosuvastatin calcium (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>183709</Austr>
				<PresentationName>Rosuvastatin GH</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROS 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183709-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183715</Austr>
				<PresentationName>Rosuvastatin GH</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROS 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183715-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183717</Austr>
				<PresentationName>Rosuvastatin GH</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROS 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183717-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183719</Austr>
				<PresentationName>Rosuvastatin GH</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>ROS</Side1Marking>
							<Side2Marking>40</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183719-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rosuvastatin calcium (Terry White Chemists)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>183058</Austr>
				<PresentationName>Terry White Chemists Rosuvastatin</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/08/2013 13:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROS 20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183058-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183062</Austr>
				<PresentationName>Terry White Chemists Rosuvastatin</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/08/2013 13:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>ROS40</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183062-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183065</Austr>
				<PresentationName>Terry White Chemists Rosuvastatin</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/08/2013 13:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROS 5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183065-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>183068</Austr>
				<PresentationName>Terry White Chemists Rosuvastatin</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/08/2013 13:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROS 10</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>183068-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rosuzet</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>203687</Austr>
				<PresentationName>Rosuzet</PresentationName>
    			<PresentionStrength>10mg+40mg</PresentionStrength>
    			<PresentationForm>Pack</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium,Ezetimibe</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Rosuzet Composite Pack</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcrosuc10821</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ezetimibe with rosuvastatin calcium</ActiveIngredient>
						<ReleaseDate>2021-08-18 14:21:19.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/09/2015 13:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>414</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>203687-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RSV 40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>203687-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>203690</Austr>
				<PresentationName>Rosuzet</PresentationName>
    			<PresentionStrength>10mg+5mg</PresentionStrength>
    			<PresentationForm>Pack</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Rosuvastatin calcium,Ezetimibe</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Rosuzet Composite Pack</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcrosuc10821</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ezetimibe with rosuvastatin calcium</ActiveIngredient>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/09/2015 13:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>414</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>203690-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RSV 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>203690-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>203692</Austr>
				<PresentationName>Rosuzet</PresentationName>
    			<PresentionStrength>10mg+20mg</PresentionStrength>
    			<PresentationForm>Pack</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ezetimibe,Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Rosuzet Composite Pack</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcrosuc10821</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ezetimibe with rosuvastatin calcium</ActiveIngredient>
						<ReleaseDate>2021-08-18 14:21:19.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/09/2015 13:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>414</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>203692-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RSV 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>203692-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>203694</Austr>
				<PresentationName>Rosuzet</PresentationName>
    			<PresentionStrength>10mg+10mg</PresentionStrength>
    			<PresentationForm>Pack</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ezetimibe,Rosuvastatin calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Rosuzet Composite Pack</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcrosuc10821</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ezetimibe with rosuvastatin calcium</ActiveIngredient>
						<ReleaseDate>2021-08-18 14:21:19.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/09/2015 13:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>414</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>203694-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RSV 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>203694-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Roxar</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>114040</Austr>
				<PresentationName>Roxar</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>114040-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>114041</Austr>
				<PresentationName>Roxar</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>114041-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Roximycin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>99937</Austr>
				<PresentationName>Roximycin</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Roxithromycin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Roximycin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcroxim11220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>roxithromycin</ActiveIngredient>
						<ReleaseDate>2020-12-22 11:18:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>150 R</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>99937-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>99939</Austr>
				<PresentationName>Roximycin</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Roxithromycin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Roximycin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcroxim11220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>roxithromycin</ActiveIngredient>
						<ReleaseDate>2020-12-22 11:18:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>300 R</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>99939-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Roxin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>93211</Austr>
				<PresentationName>Roxin</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>N F</Side1Marking>
							<Side2Marking>Arrow logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>93211-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Roxithromycin (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>133748</Austr>
				<PresentationName>Apo-Roxithromycin</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Roxithromycin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/06/2012 10:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133748-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>133749</Austr>
				<PresentationName>Apo-Roxithromycin</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Roxithromycin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/06/2012 10:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>133749-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>133749-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Roxithromycin (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>133750</Austr>
				<PresentationName>Chemmart Roxithromycin</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Roxithromycin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/06/2012 11:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133750-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>133751</Austr>
				<PresentationName>Chemmart Roxithromycin</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Roxithromycin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/06/2012 11:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>133751-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>133751-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Roxithromycin (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>154656</Austr>
				<PresentationName>Roxithromycin-GA</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 12:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>R150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154656-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>154657</Austr>
				<PresentationName>Roxithromycin-GA</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 12:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>R300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154657-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Roxithromycin (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>137902</Austr>
				<PresentationName>Roxithromycin GH</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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							<PhaseItem>1</PhaseItem>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>164 J</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>137903-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Roxithromycin (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>100989</Austr>
				<PresentationName>Roxithromycin Sandoz</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Roxithromycin</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>R 150</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>100989-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>101028</Austr>
				<PresentationName>Roxithromycin Sandoz</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Roxithromycin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 16:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>R 300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101028-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Roxithromycin (SCP)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>133756</Austr>
				<PresentationName>Roxithromycin SCP</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<VersionSequence>1</VersionSequence>
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							<Side2Marking></Side2Marking>
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			</Presentations>
			<Presentations>
				<Austr>133757</Austr>
				<PresentationName>Roxithromycin SCP</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
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							<Side2Marking></Side2Marking>
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			</Presentations>
		</Brand><Brand>
			<brandname>Roxithromycin (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>133752</Austr>
				<PresentationName>Terry White Chemists Roxithromycin</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>133753</Austr>
				<PresentationName>Terry White Chemists Roxithromycin</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
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							<Side2Marking></Side2Marking>
							<Views>
							<View>
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							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>133753-B01-01-BL600.jpg</ImageFileName>
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						</Phase>
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			</Presentations>
		</Brand><Brand>
			<brandname>Rulide</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>39409</Austr>
				<PresentationName>Rulide</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Roxithromycin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Rulide</DocumentName>
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						<VersionSequence>1</VersionSequence>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Side1Marking>164</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>42565</Austr>
				<PresentationName>Rulide</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Roxithromycin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Rulide</DocumentName>
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						<ActiveIngredient>roxithromycin</ActiveIngredient>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>164 J</Side1Marking>
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							<Views>
							<View>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>54811</Austr>
				<PresentationName>Rulide D</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Roxithromycin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Rulide D</DocumentName>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
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							<Scoring>scored</Scoring>
							<Shape>round</Shape>
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							<Side2Marking></Side2Marking>
							<Views>
							<View>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Rydapt</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>287013</Austr>
				<PresentationName>Rydapt</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>midostaurin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Rydapt</DocumentName>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>midostaurin</ActiveIngredient>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>pale orange</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>PKC NVR</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
		</Brand><Brand>
			<brandname>Rythmodan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>13537</Austr>
				<PresentationName>Rythmodan</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Disopyramide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Scoring></Scoring>
							<Shape></Shape>
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   				<WithdrawalDate></WithdrawalDate>
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			<brandname>Salazopyrin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>14485</Austr>
				<PresentationName>Salazopyrin EN</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
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							<Side1Marking>KPh</Side1Marking>
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   				<WithdrawalDate></WithdrawalDate>
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			<brandname>Salofalk</brandname>
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			<Presentations>
				<Austr>133472</Austr>
				<PresentationName>Salofalk</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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							<Side2Marking></Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Salpraz</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>169504</Austr>
				<PresentationName>Salpraz Heartburn Relief</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>21/10/2010 16:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
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							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>235309</Austr>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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							<PhaseItem>1</PhaseItem>
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							<Side2Marking></Side2Marking>
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			<brandname>Salt</brandname>
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				<Austr>10591</Austr>
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							<View>
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				<PresentationName>Samsca</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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			<brandname>Sandomigran</brandname>
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			<Presentations>
				<Austr>69608</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/04/2012 14:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>shield-shaped</Shape>
							<Side1Marking>LI100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>99038-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>99039</Austr>
				<PresentationName>Seaze</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/04/2012 14:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>shield-shaped</Shape>
							<Side1Marking>LI200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>99039-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sebifin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>149996</Austr>
				<PresentationName>Sebifin</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/02/2010 15:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>T 250</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>149996-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sebivo</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>126089</Austr>
				<PresentationName>Sebivo</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Telbivudine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/12/2008 12:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to slightly yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LDT</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>126089-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Seebri Breezhaler</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>191517</Austr>
				<PresentationName>Seebri Breezhaler</PresentationName>
    			<PresentionStrength>50mcg</PresentionStrength>
    			<PresentationForm>Inhalation Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Glycopyrronium bromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Seebri Breezhaler</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcseeih10821</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>glycopyrronium bromide (glycopyrrolate)</ActiveIngredient>
						<ReleaseDate>2021-08-25 23:46:43.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/03/2014 14:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>clear orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>company logo</Side1Marking>
							<Side2Marking>GPL 50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>191517-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Segluromet</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>287627</Austr>
				<PresentationName>Segluromet</PresentationName>
    			<PresentionStrength>7.5mg/1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>ertugliflozin pyroglutamic acid,Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Segluromet</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>mkcsemet10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ertugliflozin with metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-06-21 14:27:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/06/2019 11:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>7.5/1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>287627-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>287633</Austr>
				<PresentationName>Segluromet</PresentationName>
    			<PresentionStrength>7.5mg/500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>ertugliflozin pyroglutamic acid,Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Segluromet</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>mkcsemet10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ertugliflozin with metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-06-21 14:27:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/06/2019 11:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>7.5/500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>287633-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>287635</Austr>
				<PresentationName>Segluromet</PresentationName>
    			<PresentionStrength>2.5mg/1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>ertugliflozin pyroglutamic acid,Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Segluromet</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>mkcsemet10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ertugliflozin with metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-06-21 14:27:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/06/2019 11:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>2.5/1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>287635-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>287636</Austr>
				<PresentationName>Segluromet</PresentationName>
    			<PresentionStrength>2.5mg/500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>ertugliflozin pyroglutamic acid,Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Segluromet</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>mkcsemet10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ertugliflozin with metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-06-21 14:27:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/06/2019 11:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>2.5/500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>287636-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Selgene</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>58621</Austr>
				<PresentationName>Selgene</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Selegiline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SN 5</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>58621-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Seniere</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>163022</Austr>
				<PresentationName>Seniere</PresentationName>
    			<PresentionStrength>16mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/04/2018 13:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>163022-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Senokot</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>60850</Austr>
				<PresentationName>Senokot</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/03/2011 15:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>greenish-brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>S</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>60850-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sensipar</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>98399</Austr>
				<PresentationName>Sensipar</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Cinacalcet hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/08/2010 14:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>30</Side1Marking>
							<Side2Marking>AMG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>98399-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>98404</Austr>
				<PresentationName>Sensipar</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Cinacalcet hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/08/2010 14:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>60</Side1Marking>
							<Side2Marking>AMG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>98404-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>98407</Austr>
				<PresentationName>Sensipar</PresentationName>
    			<PresentionStrength>90mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Cinacalcet hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/08/2010 14:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>90</Side1Marking>
							<Side2Marking>AMG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>98407-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Septrin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10998</Austr>
				<PresentationName>Septrin</PresentationName>
    			<PresentionStrength>160mg/800mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>elongated</Shape>
							<Side1Marking>SEPTRIN FORTE</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10998-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sequase</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>178485</Austr>
				<PresentationName>Sequase</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/03/2012 15:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Q 25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>178485-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>178486</Austr>
				<PresentationName>Sequase</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/03/2012 15:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Q 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>178486-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>178487</Austr>
				<PresentationName>Sequase</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/03/2012 15:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Q 200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>178487-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>178488</Austr>
				<PresentationName>Sequase</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/03/2012 15:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>Q</Side1Marking>
							<Side2Marking>300</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>178488-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Serc</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>61687</Austr>
				<PresentationName>Serc</PresentationName>
    			<PresentionStrength>16mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Betahistine dihydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Serc</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocserct10322</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>betahistine dihydrochloride</ActiveIngredient>
						<ReleaseDate>2022-03-16 07:52:03.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/01/2013 16:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>267 267</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>61687-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Serenace</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10258</Austr>
				<PresentationName>Serenace</PresentationName>
    			<PresentionStrength>1.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/03/2010 11:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SIGMA</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10258-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>10259</Austr>
				<PresentationName>Serenace</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/03/2010 11:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SIGMA</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10259-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>10262</Austr>
				<PresentationName>Serenace</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/03/2010 11:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SIGMA</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10262-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Serepax</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10414</Austr>
				<PresentationName>Serepax</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>15</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10414-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>10417</Austr>
				<PresentationName>Serepax</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>30</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10417-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Seroquel</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>138917</Austr>
				<PresentationName>Seroquel XR</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/10/2008 13:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>XR 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>138917-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>138920</Austr>
				<PresentationName>Seroquel XR</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/10/2008 13:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>XR 200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>138920-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>138921</Austr>
				<PresentationName>Seroquel XR</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/10/2008 13:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>XR 300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>138921-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>138922</Austr>
				<PresentationName>Seroquel XR</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/10/2008 13:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>XR 400</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>138922-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>153883</Austr>
				<PresentationName>Seroquel XR</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/02/2010 13:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>XR 150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153883-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>58112</Austr>
				<PresentationName>Seroquel</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/05/2012 15:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Q 25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>58112-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>58113</Austr>
				<PresentationName>Seroquel</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/05/2012 15:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Q 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>58113-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>58114</Austr>
				<PresentationName>Seroquel</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/05/2012 15:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Q 200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>58114-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>78361</Austr>
				<PresentationName>Seroquel</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/05/2012 15:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>Q</Side1Marking>
							<Side2Marking>300</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>78361-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sertra</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>107067</Austr>
				<PresentationName>Sertra</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SR 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>107067-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>107071</Austr>
				<PresentationName>Sertra</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SR 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>107071-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sertracor</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>147077</Austr>
				<PresentationName>Sertracor</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/11/2013 15:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>SER</Side1Marking>
							<Side2Marking>50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>147077-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>147078</Austr>
				<PresentationName>Sertracor</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/11/2013 15:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>SER</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>147078-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sertraline (Actavis)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>195321</Austr>
				<PresentationName>Sertraline Actavis</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 15:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>100 BL</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195321-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>195322</Austr>
				<PresentationName>Sertraline Actavis</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 15:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>50 BL</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195322-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sertraline (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>195315</Austr>
				<PresentationName>Sertraline AN</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/10/2017 13:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>50 BL</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195315-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>195326</Austr>
				<PresentationName>Sertraline AN</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/10/2017 13:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>100 BL</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195326-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sertraline (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>213177</Austr>
				<PresentationName>APO-Sertraline</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sertraline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 10:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>50 BL</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>213177-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>213180</Austr>
				<PresentationName>APO-Sertraline</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sertraline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 10:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>100 BL</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>213180-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sertraline (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>213178</Austr>
				<PresentationName>Chemmart Sertraline</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sertraline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>50 BL</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>213178-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>213181</Austr>
				<PresentationName>Chemmart Sertraline</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sertraline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>100 BL</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>213181-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sertraline (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>124855</Austr>
				<PresentationName>Sertraline generichealth</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/04/2012 23:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>SER</Side1Marking>
							<Side2Marking>5 0</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>124855-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>124856</Austr>
				<PresentationName>Sertraline generichealth</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/04/2012 23:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>SER</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>124856-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sertraline (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>130617</Austr>
				<PresentationName>Pharmacor Sertraline</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/08/2009 13:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>bluish purple</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SE 50</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>130617-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>130618</Austr>
				<PresentationName>Pharmacor Sertraline</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/08/2009 13:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SER 100</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>130618-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sertraline (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>98697</Austr>
				<PresentationName>Sertraline Sandoz</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sertraline</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/04/2011 15:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>SE 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>98697-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>98698</Austr>
				<PresentationName>Sertraline Sandoz</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sertraline</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/04/2011 15:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>SE 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>98698-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sertraline (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>213179</Austr>
				<PresentationName>Terry White Chemists Sertraline</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sertraline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>50 BL</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>213179-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>213182</Austr>
				<PresentationName>Terry White Chemists Sertraline</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sertraline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>100 BL</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>213182-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sertraline-WT</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>124853</Austr>
				<PresentationName>Sertraline-WT</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 13:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>SER</Side1Marking>
							<Side2Marking>50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>124853-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>124854</Austr>
				<PresentationName>Sertraline-WT</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 13:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>SER</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>124854-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Setacol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>78380</Austr>
				<PresentationName>Setacol</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2010 16:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>78380-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Setrona</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>116623</Austr>
				<PresentationName>Setrona</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 10:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>caplet</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>116623-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>116636</Austr>
				<PresentationName>Setrona</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 10:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>caplet</Shape>
							<Side1Marking>100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>116636-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sevelamer (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>286648</Austr>
				<PresentationName>Sevelamer (Apotex)</PresentationName>
    			<PresentionStrength>800mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/02/2021 13:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>R789</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>286648-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sevikar</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>157562</Austr>
				<PresentationName>Sevikar</PresentationName>
    			<PresentionStrength>40mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olmesartan medoxomil,Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sevikar</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcsevik10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>olmesartan medoxomil with amlodipine besilate</ActiveIngredient>
						<ReleaseDate>2022-08-17 17:33:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>05/01/2011 16:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brownish-red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C77</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157562-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>157563</Austr>
				<PresentationName>Sevikar</PresentationName>
    			<PresentionStrength>40mg/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olmesartan medoxomil,Amlodipine besylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sevikar</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcsevik10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>olmesartan medoxomil with amlodipine besilate</ActiveIngredient>
						<ReleaseDate>2022-08-17 17:33:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>05/01/2011 16:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>cream</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C75</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157563-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>157565</Austr>
				<PresentationName>Sevikar</PresentationName>
    			<PresentionStrength>20mg/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besylate,Olmesartan medoxomil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sevikar</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcsevik10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>olmesartan medoxomil with amlodipine besilate</ActiveIngredient>
						<ReleaseDate>2022-08-17 17:33:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>05/01/2011 16:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C73</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157565-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sevikar HCT</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>198998</Austr>
				<PresentationName>Sevikar HCT</PresentationName>
    			<PresentionStrength>20mg/5mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Amlodipine besilate,Olmesartan medoxomil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sevikar HCT</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcsvhct10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>olmesartan medoxomil with amlodipine besilate and hydrochlorothiazide</ActiveIngredient>
						<ReleaseDate>2022-08-31 09:24:55.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/09/2014 11:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C51</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>198998-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199000</Austr>
				<PresentationName>Sevikar HCT</PresentationName>
    			<PresentionStrength>40mg/10mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besilate,Hydrochlorothiazide,Olmesartan medoxomil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sevikar HCT</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcsvhct10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>olmesartan medoxomil with amlodipine besilate and hydrochlorothiazide</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/09/2014 11:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>greyish red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C57</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199000-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199005</Austr>
				<PresentationName>Sevikar HCT</PresentationName>
    			<PresentionStrength>40mg/10mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besilate,Hydrochlorothiazide,Olmesartan medoxomil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sevikar HCT</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcsvhct10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>olmesartan medoxomil with amlodipine besilate and hydrochlorothiazide</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/09/2014 11:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>greyish red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C55</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199005-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199006</Austr>
				<PresentationName>Sevikar HCT</PresentationName>
    			<PresentionStrength>40mg/5mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olmesartan medoxomil,Amlodipine besilate,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sevikar HCT</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcsvhct10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>olmesartan medoxomil with amlodipine besilate and hydrochlorothiazide</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/09/2014 11:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C53</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199006-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199007</Austr>
				<PresentationName>Sevikar HCT</PresentationName>
    			<PresentionStrength>40mg/5mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amlodipine besilate,Hydrochlorothiazide,Olmesartan medoxomil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sevikar HCT</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>olmesartan medoxomil with amlodipine besilate and hydrochlorothiazide</ActiveIngredient>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/09/2014 12:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C54</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199007-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sevredol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>214089</Austr>
				<PresentationName>Sevredol</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Morphine sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/03/2015 10:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>IR 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>214089-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>47543</Austr>
				<PresentationName>Sevredol</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Morphine sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/08/2010 09:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>IR 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>47543-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sical</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>126438</Austr>
				<PresentationName>Sical</PresentationName>
    			<PresentionStrength>0.25mcg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Calcitriol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
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						<DateEffective>31/12/2010 11:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
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							<Scoring></Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>126438-C01-02-BL600.jpg</ImageFileName>
							</View>
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						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>236776</Austr>
				<PresentationName>Sical</PresentationName>
    			<PresentionStrength>0.25mcg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Calcitriol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sical</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
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						<ActiveIngredient>calcitriol</ActiveIngredient>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>26/10/2016 14:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
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							<Scoring></Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
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			</Presentations>
		</Brand><Brand>
			<brandname>Sifrol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>158754</Austr>
				<PresentationName>Sifrol ER</PresentationName>
    			<PresentionStrength>0.375mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>pramipexole dihydrochloride monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sifrol ER</DocumentName>
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							<DocumentType>eCMI</DocumentType>
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						<ActiveIngredient>pramipexole dihydrochloride</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>19/11/2011 10:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>P1</Side1Marking>
							<Side2Marking>Company Symbol</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158754-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>158755</Austr>
				<PresentationName>Sifrol ER</PresentationName>
    			<PresentionStrength>0.75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
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			<Presentations>
				<Austr>164810</Austr>
				<PresentationName>APO-Sildenafil PHT</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sildenafil citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 10:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SIL 20</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>164810-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>164811</Austr>
				<PresentationName>APO-Sildenafil</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sildenafil citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/09/2014 11:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>diamond-shaped</Shape>
							<Side1Marking>SIL25</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>164811-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>164813</Austr>
				<PresentationName>APO-Sildenafil</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sildenafil citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/09/2014 11:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>diamond-shaped</Shape>
							<Side1Marking>SIL50</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>164813-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>186284</Austr>
				<PresentationName>Sildenafil Apotex</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/03/2020 20:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SC</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>186284-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>186284-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>186292</Austr>
				<PresentationName>Sildenafil Apotex</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/03/2020 20:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SC</Side1Marking>
							<Side2Marking>50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>186292-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>186300</Austr>
				<PresentationName>Sildenafil Apotex</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/03/2020 20:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SC</Side1Marking>
							<Side2Marking>25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>186300-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sildenafil citrate (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>164814</Austr>
				<PresentationName>Chemmart Sildenafil</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sildenafil citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/09/2014 11:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>diamond-shaped</Shape>
							<Side1Marking>SIL25</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>164814-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>164816</Austr>
				<PresentationName>Chemmart Sildenafil</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sildenafil citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/09/2014 11:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>diamond-shaped</Shape>
							<Side1Marking>SIL50</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>164816-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>164821</Austr>
				<PresentationName>Chemmart Sildenafil</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sildenafil citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/09/2014 11:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>diamond-shaped</Shape>
							<Side1Marking>SIL100</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>164821-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sildenafil citrate (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>186299</Austr>
				<PresentationName>Sildenafil generichealth</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/05/2017 17:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SC</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>186299-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>186299-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sildenafil citrate (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>148567</Austr>
				<PresentationName>Sildenafil Sandoz</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sildenafil citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue slightly dotted</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>148567-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>148568</Austr>
				<PresentationName>Sildenafil Sandoz</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sildenafil citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue slightly dotted</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>148568-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>148568-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>148570</Austr>
				<PresentationName>Sildenafil Sandoz</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sildenafil citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue slightly dotted</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>148570-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>188702</Austr>
				<PresentationName>Sildenafil Sandoz PHT 20</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/12/2014 13:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>188702-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sildenafil citrate (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>164815</Austr>
				<PresentationName>Terry White Chemists Sildenafil</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sildenafil citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/09/2014 11:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>diamond-shaped</Shape>
							<Side1Marking>SIL25</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>164815-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>164818</Austr>
				<PresentationName>Terry White Chemists Sildenafil</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sildenafil citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/09/2014 11:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>diamond-shaped</Shape>
							<Side1Marking>SIL100</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
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			<Presentations>
				<Austr>164820</Austr>
				<PresentationName>Terry White Chemists Sildenafil</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Side1Marking>SIL50</Side1Marking>
							<Side2Marking>APO</Side2Marking>
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			<brandname>Simipex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>172017</Austr>
				<PresentationName>Simipex</PresentationName>
    			<PresentionStrength>0.125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
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							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>172018</Austr>
				<PresentationName>Simipex</PresentationName>
    			<PresentionStrength>0.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>B</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>172018-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
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			</Presentations>
			<Presentations>
				<Austr>172021</Austr>
				<PresentationName>Simipex</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>D</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>172021-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>225573</Austr>
				<PresentationName>Simipex XR</PresentationName>
    			<PresentionStrength>0.75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>10/07/2018 11:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white or nearly white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>cylindrical</Shape>
							<Side1Marking>052</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>225573-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>225578</Austr>
				<PresentationName>Simipex XR</PresentationName>
    			<PresentionStrength>3.75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>10/07/2018 11:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white or nearly white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>cylindrical</Shape>
							<Side1Marking>262</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>225578-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>225603</Austr>
				<PresentationName>Simipex XR</PresentationName>
    			<PresentionStrength>1.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>10/07/2018 11:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white or nearly white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>cylindrical</Shape>
							<Side1Marking>105</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>225603-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>225605</Austr>
				<PresentationName>Simipex XR</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>10/07/2018 11:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white or nearly white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>cylindrical</Shape>
							<Side1Marking>210</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>225605-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>225628</Austr>
				<PresentationName>Simipex XR </PresentationName>
    			<PresentionStrength>4.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white or nearly white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>cylindrical</Shape>
							<Side1Marking>315</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>225628-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Simpral</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>173137</Austr>
				<PresentationName>Simpral</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pramipexole hydrochloride monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<QualiferData></QualiferData>
						<DocumentName>Simpral</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
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								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>pramipexole dihydrochloride</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/11/2016 15:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>M PX4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>173137-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>173138</Austr>
				<PresentationName>Simpral</PresentationName>
    			<PresentionStrength>0.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pramipexole hydrochloride monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Simpral</DocumentName>
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						<ActiveIngredient>pramipexole dihydrochloride</ActiveIngredient>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>PX2</Side1Marking>
							<Side2Marking>M</Side2Marking>
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			</Presentations>
			<Presentations>
				<Austr>173139</Austr>
				<PresentationName>Simpral</PresentationName>
    			<PresentionStrength>0.125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Pramipexole hydrochloride monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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						<ActiveIngredient>pramipexole dihydrochloride</ActiveIngredient>
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						<DateEffective>07/11/2016 15:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PX1</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>173139-C01-01-BL600.jpg</ImageFileName>
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		</Brand><Brand>
			<brandname>Simvacor</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>182906</Austr>
				<PresentationName>Simvacor</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateEffective>11/10/2013 11:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SVN10</Side1Marking>
							<Side2Marking>NEO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>182907</Austr>
				<PresentationName>Simvacor</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>tan</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SVN20</Side1Marking>
							<Side2Marking>NEO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>182907-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>182908</Austr>
				<PresentationName>Simvacor</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>13/12/2011 09:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SVN 40</Side1Marking>
							<Side2Marking>NEO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>182908-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>182909</Austr>
				<PresentationName>Simvacor</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
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    			<TGAIngredient></TGAIngredient>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<brandname>Simvastatin (Amneal)</brandname>
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				<Austr>170525</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
				<Austr>170526</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
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							<Views>
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			</Presentations>
			<Presentations>
				<Austr>170527</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
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							<Side1Marking>A</Side1Marking>
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			<Presentations>
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		</Brand><Brand>
			<brandname>Simvastatin (Apotex)</brandname>
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				<Austr>149812</Austr>
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							<Side1Marking>10</Side1Marking>
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			<Presentations>
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			<Presentations>
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			<Presentations>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>SVN 80</Side1Marking>
							<Side2Marking>NEO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>223451-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Simvastatin (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>211956</Austr>
				<PresentationName>Chemmart Simvastatin</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SVN 10</Side1Marking>
							<Side2Marking>NEO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>211956-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>211957</Austr>
				<PresentationName>Chemmart Simvastatin</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>tan</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SVN 20</Side1Marking>
							<Side2Marking>NEO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>211957-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>211958</Austr>
				<PresentationName>Chemmart Simvastatin</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:14</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SVN 40</Side1Marking>
							<Side2Marking>NEO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>211958-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>211959</Austr>
				<PresentationName>Chemmart Simvastatin</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>SVN 80</Side1Marking>
							<Side2Marking>NEO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>211959-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Simvastatin (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>199743</Austr>
				<PresentationName>Simvastatin-GA</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 12:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>shield-shaped</Shape>
							<Side1Marking>SV 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199743-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199744</Austr>
				<PresentationName>Simvastatin-GA</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 12:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>tan</Colour>
							<Scoring>unscored</Scoring>
							<Shape>shield-shaped</Shape>
							<Side1Marking>SV 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199744-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199745</Austr>
				<PresentationName>Simvastatin-GA</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 12:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>shield-shaped</Shape>
							<Side1Marking>SV 40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199745-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199746</Austr>
				<PresentationName>Simvastatin-GA</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 12:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>SV 80</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199746-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Simvastatin (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>123813</Austr>
				<PresentationName>Simvastatin generichealth</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/09/2011 15:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>123813-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>123815</Austr>
				<PresentationName>Simvastatin generichealth</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/11/2008 17:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>tan</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>123815-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>123817</Austr>
				<PresentationName>Simvastatin generichealth</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/11/2008 17:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brick-red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>123817-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>123819</Austr>
				<PresentationName>Simvastatin generichealth</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/11/2008 17:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brick-red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>123</Side1Marking>
							<Side2Marking>80</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>123819-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Simvastatin (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>114796</Austr>
				<PresentationName>Simvastatin Sandoz</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 14:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SIM 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>114796-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>114797</Austr>
				<PresentationName>Simvastatin Sandoz</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 14:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SIM 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>114797-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>114798</Austr>
				<PresentationName>Simvastatin Sandoz</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 14:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SIM 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>114798-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>114800</Austr>
				<PresentationName>Simvastatin Sandoz</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 14:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SIM 40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>114800-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>98624</Austr>
				<PresentationName>Simvastatin Sandoz</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/09/2008 14:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light green</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SIM 80</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>98624-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Simvastatin (Spirit)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>116701</Austr>
				<PresentationName>Simvastatin-Spirit</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2011 12:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>shield-shaped</Shape>
							<Side1Marking>SV 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>116701-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>116702</Austr>
				<PresentationName>Simvastatin-Spirit</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2011 12:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>tan</Colour>
							<Scoring>unscored</Scoring>
							<Shape>shield-shaped</Shape>
							<Side1Marking>SV 20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>116702-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>116704</Austr>
				<PresentationName>Simvastatin-Spirit</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2011 12:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>shield-shaped</Shape>
							<Side1Marking>SV 40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>116704-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>116705</Austr>
				<PresentationName>Simvastatin-Spirit</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2011 12:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>SV 80</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>116705-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Simvastatin (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>211952</Austr>
				<PresentationName>Terry White Chemists Simvastatin</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SVN 10</Side1Marking>
							<Side2Marking>NEO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>211952-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>211953</Austr>
				<PresentationName>Terry White Chemists Simvastatin</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>tan</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SVN 20</Side1Marking>
							<Side2Marking>NEO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>211953-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>211954</Austr>
				<PresentationName>Terry White Chemists Simvastatin</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SVN 40</Side1Marking>
							<Side2Marking>NEO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>211954-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>211955</Austr>
				<PresentationName>Terry White Chemists Simvastatin</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 11:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>SVN 80</Side1Marking>
							<Side2Marking>NEO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>211955-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sinadopa</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>275974</Austr>
				<PresentationName>Sinadopa</PresentationName>
    			<PresentionStrength>100mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>04/06/2020 11:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C</Side1Marking>
							<Side2Marking>19</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>275974-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>275983</Austr>
				<PresentationName>Sinadopa</PresentationName>
    			<PresentionStrength>250mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/06/2020 11:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>275983-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sinemet</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>171665</Austr>
				<PresentationName>Sinemet</PresentationName>
    			<PresentionStrength>100/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Levodopa,Carbidopa</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/03/2012 10:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>650</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>171665-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>171666</Austr>
				<PresentationName>Sinemet</PresentationName>
    			<PresentionStrength>250/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Levodopa,Carbidopa</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>18/05/2012 15:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light dappled blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>654</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>171666-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>319330</Austr>
				<PresentationName>Sinemet</PresentationName>
    			<PresentionStrength>100mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>levodopa,carbidopa monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sinemet</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levodopa with carbidopa monohydrate</ActiveIngredient>
						<ReleaseDate>2021-04-14 13:59:05.0</ReleaseDate>
					</DocumentQualifiers>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/01/2021 10:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>650</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>319330-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>319331</Austr>
				<PresentationName>Sinemet</PresentationName>
    			<PresentionStrength>250mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>levodopa,carbidopa monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sinemet</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levodopa with carbidopa monohydrate</ActiveIngredient>
						<ReleaseDate>2021-04-14 13:59:05.0</ReleaseDate>
					</DocumentQualifiers>
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				<Images>
					<Versions>
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						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/01/2021 10:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light dappled blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>654</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>319331-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>326195</Austr>
				<PresentationName>Sinemet CR</PresentationName>
    			<PresentionStrength>200mg/50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>carbidopa monohydrate,levodopa</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Sinemet CR 200/50</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amisulpride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Solian</DocumentName>
						<DocumentTypes>
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								<Format>PDF</Format>
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							</AvailableFormats>
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						<ActiveIngredient>amisulpride</ActiveIngredient>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/07/2008 13:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AMI 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96422-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>96425</Austr>
				<PresentationName>Solian</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amisulpride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Solian</DocumentName>
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								<Format>PDF</Format>
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						<ActiveIngredient>amisulpride</ActiveIngredient>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AMI 200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>96425-A01-01-BL600.jpg</ImageFileName>
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							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>96425-B01-01-BL600.jpg</ImageFileName>
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							</Views>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Solicare</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>296740</Austr>
				<PresentationName>Solicare</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
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							<Shape>round</Shape>
							<Side1Marking>EG</Side1Marking>
							<Side2Marking>1</Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>296740-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>296746</Austr>
				<PresentationName>Solicare</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
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							<Shape>round</Shape>
							<Side1Marking>EG</Side1Marking>
							<Side2Marking>2</Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>316984</Austr>
				<PresentationName>Solicare ODT</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>316984-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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			</Presentations>
			<Presentations>
				<Austr>316987</Austr>
				<PresentationName>Solicare ODT</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>316987-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Solone</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>13468</Austr>
				<PresentationName>Solone</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Prednisolone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Solone</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
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						<ActiveIngredient>prednisolone</ActiveIngredient>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/03/2010 11:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
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							<Views>
							<View>
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							</Views>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>13469</Austr>
				<PresentationName>Solone</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Prednisolone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Solone</DocumentName>
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								<Format>PDF</Format>
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						<ActiveIngredient>prednisolone</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>18/08/2017 10:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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			</Presentations>
		</Brand><Brand>
			<brandname>Solprin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>59902</Austr>
				<PresentationName>Solprin</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/03/2011 12:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SOLPRIN sword</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>59902-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>59902-B01-01-BL600.jpg</ImageFileName>
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							</Views>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Somac</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>154252</Austr>
				<PresentationName>Somac Heartburn Relief</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>pantoprazole</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			</Presentations>
			<Presentations>
				<Austr>234279</Austr>
				<PresentationName>Somac Heartburn Relief</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>pantoprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Side2Marking></Side2Marking>
							<Views>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>69792</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>pantoprazole sodium sesquihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Somac</DocumentName>
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						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
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				</Images>
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			<Presentations>
				<Austr>70829</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>pantoprazole sodium sesquihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<QualiferData></QualiferData>
						<DocumentName>Somac</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>pantoprazole sodium</ActiveIngredient>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Side2Marking></Side2Marking>
							<Views>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Somidem</brandname>
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			<Presentations>
				<Austr>119196</Austr>
				<PresentationName>Somidem</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Zolpidem tartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Somidem</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcsomid11121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>zolpidem tartrate</ActiveIngredient>
						<ReleaseDate>2021-11-05 07:36:32.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>ZM 10</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>119196-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sone</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>13470</Austr>
				<PresentationName>Sone</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Prednisone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sone</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>iacsonee10621</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>prednisone</ActiveIngredient>
						<ReleaseDate>2021-06-23 14:44:26.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>13470-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>56129</Austr>
				<PresentationName>Sone</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Prednisone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sone</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>iacsonee10621</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>prednisone</ActiveIngredient>
						<ReleaseDate>2021-06-23 14:44:26.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>56129-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sotacor</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>68966</Austr>
				<PresentationName>Sotacor</PresentationName>
    			<PresentionStrength>160mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/08/2018 12:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>S 160</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>68966-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sotalol Hydrochloride (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>73846</Austr>
				<PresentationName>APO-Sotalol</PresentationName>
    			<PresentionStrength>160mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Sotalol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/08/2008 09:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>APO-160</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73846-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>83094</Austr>
				<PresentationName>APO-Sotalol</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Sotalol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/08/2008 09:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>APO-80</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>83094-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sotalol Hydrochloride (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>63724</Austr>
				<PresentationName>Sotalol Sandoz</PresentationName>
    			<PresentionStrength>160mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sotalol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 14:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SOT</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>63724-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>78710</Austr>
				<PresentationName>Sotalol Sandoz</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sotalol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/02/2018 14:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SOT</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>78710-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sozol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>191035</Austr>
				<PresentationName>Sozol</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/08/2018 12:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow to pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>191035-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Span K</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>27978</Austr>
				<PresentationName>Span-K</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Potassium chloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/11/2008 13:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>27978-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>27978-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Spedra</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>228474</Austr>
				<PresentationName>Spedra</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>avanafil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Spedra</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>avanafil</ActiveIngredient>
						<ReleaseDate>2018-12-20 15:01:04.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2019 11:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>228474-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>228475</Austr>
				<PresentationName>Spedra</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>avanafil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Spedra</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>avanafil</ActiveIngredient>
						<ReleaseDate>2018-12-20 15:01:04.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2019 11:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>228475-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>228476</Austr>
				<PresentationName>Spedra</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>avanafil</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Spedra</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>avanafil</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/03/2019 11:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>228476-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Spiractin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>46689</Austr>
				<PresentationName>Spiractin</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Spironolactone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Spiractin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcspira11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>spironolactone</ActiveIngredient>
						<ReleaseDate>2022-10-12 14:22:35.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SP 1</Side1Marking>
							<Side2Marking>&#945;</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>46689-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>46691</Austr>
				<PresentationName>Spiractin</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Spironolactone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Spiractin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>spironolactone</ActiveIngredient>
						<ReleaseDate>2022-10-12 14:22:35.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SP 2</Side1Marking>
							<Side2Marking>&#945;</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>46691-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Spiriva</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>81525</Austr>
				<PresentationName>Spiriva</PresentationName>
    			<PresentionStrength>18mcg</PresentionStrength>
    			<PresentationForm>Inhalation Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>tiotropium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Spiriva</DocumentName>
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							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tiotropium bromide monohydrate</ActiveIngredient>
						<ReleaseDate>2021-07-06 15:08:07.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>11/01/2010 09:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Boehringer Ingelheim Logo</Side1Marking>
							<Side2Marking>TI 01</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>81525-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Spironolactone (Viatris)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>338091</Austr>
				<PresentationName>Spironolactone Viatris</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>spironolactone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Spironolactone Viatris</DocumentName>
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							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcspiro11022</Filename>
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						</DocumentTypes>
						<ActiveIngredient>spironolactone</ActiveIngredient>
						<ReleaseDate>2022-10-12 14:21:44.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/11/2022 12:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SP 1</Side1Marking>
							<Side2Marking>&#945;</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>338091-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>338092</Austr>
				<PresentationName>Spironolactone Viatris</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>spironolactone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Spironolactone Viatris</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcspiro11022</Filename>
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						</DocumentTypes>
						<ActiveIngredient>spironolactone</ActiveIngredient>
						<ReleaseDate>2022-10-12 14:21:44.0</ReleaseDate>
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				<Images>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/11/2022 12:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SP 2</Side1Marking>
							<Side2Marking>&#945;</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>338092-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Sporanox</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>47012</Austr>
				<PresentationName>Sporanox Capsules</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sporanox Capsules</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>itraconazole</ActiveIngredient>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/07/2008 09:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>pink and blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>47012-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Stalevo</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>146890</Austr>
				<PresentationName>Stalevo</PresentationName>
    			<PresentionStrength>200/50/200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Entacapone,Carbidopa,Levodopa</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/05/2009 13:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark brownish-red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LCE 200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>146890-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>160686</Austr>
				<PresentationName>Stalevo</PresentationName>
    			<PresentionStrength>75/18.75/200mg</PresentionStrength>
    			<PresentationForm>Tablets </PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Entacapone,Levodopa,Carbidopa</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/01/2011 13:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light brownish red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LCE75</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>160686-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>160687</Austr>
				<PresentationName>Stalevo</PresentationName>
    			<PresentionStrength>125/31.25/200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Entacapone,Levodopa,Carbidopa</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/01/2011 13:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light brownish red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LCE 125</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>160687-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
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			</Presentations>
			<Presentations>
				<Austr>96372</Austr>
				<PresentationName>Stalevo</PresentationName>
    			<PresentionStrength>50/12.5/200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Levodopa,Carbidopa,Entacapone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>10/12/2008 11:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brownish red, greyish red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>LCE 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96372-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
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			</Presentations>
			<Presentations>
				<Austr>96395</Austr>
				<PresentationName>Stalevo</PresentationName>
    			<PresentionStrength>100/25/200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Entacapone,Levodopa,Carbidopa</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>10/12/2008 11:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brownish red, greyish red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>LCE 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96395-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>96396</Austr>
				<PresentationName>Stalevo</PresentationName>
    			<PresentionStrength>150/37.5/200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Entacapone,Levodopa,Carbidopa</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>10/12/2008 11:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brownish red, greyish red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>ellipse-shaped</Shape>
							<Side1Marking>LCE 150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96396-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Staphylex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>17683</Austr>
				<PresentationName>Staphylex</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Flucloxacillin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Staphylex</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>flucloxacillin sodium monohydrate</ActiveIngredient>
						<ReleaseDate>2022-07-26 10:59:40.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow and black</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>17683-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>17684</Austr>
				<PresentationName>Staphylex</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Flucloxacillin sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Staphylex</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcstaph10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>flucloxacillin sodium monohydrate</ActiveIngredient>
						<ReleaseDate>2022-07-26 10:59:40.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow and black</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>17684-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
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			<brandname>Steglatro</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>287619</Austr>
				<PresentationName>Steglatro</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<QualiferData></QualiferData>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
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							<Shape>triangular</Shape>
							<Side1Marking>701</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>287619-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>287622</Austr>
				<PresentationName>Steglatro</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>ertugliflozin pyroglutamic acid</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<QualiferData></QualiferData>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Steglujan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>287626</Austr>
				<PresentationName>Steglujan</PresentationName>
    			<PresentionStrength>15mg/100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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			</Presentations>
			<Presentations>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>ertugliflozin pyroglutamic acid,sitagliptin phosphate monohydrate</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<DocumentQualifiers>
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						<DocumentName>Steglujan</DocumentName>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
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							<Side1Marking>554</Side1Marking>
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			</Presentations>
		</Brand><Brand>
			<brandname>Stelax</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>92251</Austr>
				<PresentationName>Stelax</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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							<Shape>round</Shape>
							<Side1Marking>BL 10</Side1Marking>
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							<Views>
							<View>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Stelazine</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>66873</Austr>
				<PresentationName>Stelazine</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Side2Marking></Side2Marking>
							<Views>
							<View>
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				</Images>
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			<Presentations>
				<Austr>66874</Austr>
				<PresentationName>Stelazine</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
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							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>66874-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>66875</Austr>
				<PresentationName>Stelazine</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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								<ImageFileName>66875-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Stemetil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>27564</Austr>
				<PresentationName>Stemetil</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Prochlorperazine maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Stemetil</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
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						<ActiveIngredient>prochlorperazine; prochlorperazine maleate; prochlorperazine mesilate</ActiveIngredient>
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				<Images>
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						<DateEffective>24/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
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			</Presentations>
		</Brand><Brand>
			<brandname>Stemzine</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>67940</Austr>
				<PresentationName>Stemzine</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Prochlorperazine maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<DocumentQualifiers>
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							<AvailableFormats>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Shape>round</Shape>
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							<Views>
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			<brandname>Stildem</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>120379</Austr>
				<PresentationName>Stildem</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>Z 10</Side1Marking>
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							<Views>
							<View>
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			</Presentations>
		</Brand><Brand>
			<brandname>Stilnox</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>120707</Austr>
				<PresentationName>Stilnox CR</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Zolpidem tartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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							<AvailableFormats>
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						<ActiveIngredient>zolpidem tartrate</ActiveIngredient>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<Side1Marking>ZMR</Side1Marking>
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							<Views>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>120713</Austr>
				<PresentationName>Stilnox CR</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Zolpidem tartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Stilnox CR</DocumentName>
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							<AvailableFormats>
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						<ActiveIngredient>zolpidem tartrate</ActiveIngredient>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>69681</Austr>
				<PresentationName>Stilnox</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Zolpidem tartrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Stilnox</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcstiln10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>zolpidem tartrate</ActiveIngredient>
						<ReleaseDate>2022-06-06 09:04:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/01/2009 14:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>SN 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>69681-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Stocrin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>125199</Austr>
				<PresentationName>Stocrin</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Efavirenz</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Stocrin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>mkcstocr14222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>efavirenz</ActiveIngredient>
						<ReleaseDate>2022-02-22 15:35:38.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 12:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>223</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>125199-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>82789</Austr>
				<PresentationName>Stocrin</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Efavirenz</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Stocrin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>mkcstocr14222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>efavirenz</ActiveIngredient>
						<ReleaseDate>2022-02-22 15:35:38.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/09/2008 10:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified capsular-shaped</Shape>
							<Side1Marking>225</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82789-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Stop-It</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>199731</Austr>
				<PresentationName>Stop-It</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>grey and green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199731-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Strattera</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>146333</Austr>
				<PresentationName>Strattera</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atomoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Strattera</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>lycstrat11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>atomoxetine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-14 17:03:09.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/07/2009 13:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque brown and opaque white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Lilly 3250</Side1Marking>
							<Side2Marking>80 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>146333-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>146413</Austr>
				<PresentationName>Strattera</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atomoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Strattera</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>lycstrat11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>atomoxetine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-14 17:03:09.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/07/2009 13:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque brown</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Lilly 3251</Side1Marking>
							<Side2Marking>100 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>146413-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>90592</Austr>
				<PresentationName>Strattera</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atomoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Strattera</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>lycstrat11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>atomoxetine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-14 17:03:09.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/07/2009 13:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Lilly 3227</Side1Marking>
							<Side2Marking>10 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>90592-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>90593</Austr>
				<PresentationName>Strattera</PresentationName>
    			<PresentionStrength>18mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atomoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Strattera</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>lycstrat11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>atomoxetine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-14 17:03:09.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/07/2009 13:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>gold and opaque white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Lilly 3238</Side1Marking>
							<Side2Marking>18 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>90593-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>90594</Austr>
				<PresentationName>Strattera</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atomoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Strattera</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>lycstrat11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>atomoxetine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-14 17:03:09.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/07/2009 13:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque blue and opaque white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Lilly 3228</Side1Marking>
							<Side2Marking>25 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>90594-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>90595</Austr>
				<PresentationName>Strattera</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atomoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Strattera</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>lycstrat11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>atomoxetine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-14 17:03:09.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/07/2009 13:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Lilly 3229</Side1Marking>
							<Side2Marking>40 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>90595-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>90596</Austr>
				<PresentationName>Strattera</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atomoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Strattera</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>lycstrat11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>atomoxetine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-14 17:03:09.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/07/2009 13:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque blue and gold</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Lilly 3239</Side1Marking>
							<Side2Marking>60 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>90596-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Stromectol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>181338</Austr>
				<PresentationName>Stromectol</PresentationName>
    			<PresentionStrength>3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Ivermectin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Stromectol blister pack</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>mkcstrob10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ivermectin</ActiveIngredient>
						<ReleaseDate>2022-03-03 10:33:34.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/10/2011 14:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>32</Side1Marking>
							<Side2Marking>MSD</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>181338-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Subutex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>76661</Austr>
				<PresentationName>Subutex</PresentationName>
    			<PresentionStrength>0.4mg</PresentionStrength>
    			<PresentationForm>Sublingual tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Buprenorphine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Subutex</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ircsubtx10421</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>buprenorphine hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-04-13 10:02:13.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/02/2017 10:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>04</Side1Marking>
							<Side2Marking> </Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>76661-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>76662</Austr>
				<PresentationName>Subutex</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Sublingual tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Buprenorphine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Subutex</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ircsubtx10421</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>buprenorphine hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-04-13 10:02:13.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/02/2017 10:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>B2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>76662-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>76663</Austr>
				<PresentationName>Subutex</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Sublingual tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Buprenorphine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Subutex</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ircsubtx10421</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>buprenorphine hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-04-13 10:02:13.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/12/2016 13:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>B8</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>76663-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sudafed PE</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>115775</Austr>
				<PresentationName>Sudafed PE</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/09/2016 14:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red-brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>PE</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>115775-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sudafed Sinus</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>40335</Austr>
				<PresentationName>Sudafed Sinus + Allergy &amp; Pain Relief Tablets</PresentationName>
    			<PresentionStrength>30mg/500mg/1.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sudafed Sinus + Allergy &amp; Pain Relief Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pccsudap40522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>paracetamol  with pseudoephedrine hydrochloride and triprolidine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-06-06 09:14:45.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/09/2016 15:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>turquoise</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>S3F S3F</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>40335-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>63230</Austr>
				<PresentationName>Sudafed Sinus + Pain Relief Tablets</PresentationName>
    			<PresentionStrength>30mg/500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sudafed Sinus + Pain Relief Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pccsudpr40122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>paracetamol with pseudoephedrine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-04-13 09:55:54.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/09/2016 15:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>P3F</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>63230-A01-01-BL600.jpg</ImageFileName>
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							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>63230-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sulprix</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>152460</Austr>
				<PresentationName>Sulprix</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amisulpride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sulprix</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcsulpr20522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amisulpride</ActiveIngredient>
						<ReleaseDate>2022-05-17 12:55:39.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/07/2010 16:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>AS 400</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>152460-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156044</Austr>
				<PresentationName>Sulprix</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amisulpride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sulprix</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcsulpr20522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amisulpride</ActiveIngredient>
						<ReleaseDate>2022-05-17 12:55:39.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/07/2010 16:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AMI 100</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156048</Austr>
				<PresentationName>Sulprix</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Amisulpride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Sulprix</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amisulpride</ActiveIngredient>
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				<Images>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AMI 200</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156048-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sumagran</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>117670</Austr>
				<PresentationName>Sumagran</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SA 50</Side1Marking>
							<Side2Marking>Arrow logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>117670-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>117727</Austr>
				<PresentationName>Sumagran</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SA 100</Side1Marking>
							<Side2Marking>Arrow logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>117727-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>117727-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sumatran</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>187216</Austr>
				<PresentationName>Sumatran</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/08/2018 12:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>187216-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>187217</Austr>
				<PresentationName>Sumatran</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>187217-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
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			</Presentations>
		</Brand><Brand>
			<brandname>Sumatriptan (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>160188</Austr>
				<PresentationName>APO-Sumatriptan</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sumatriptan succinate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/03/2011 10:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>160188-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>160196</Austr>
				<PresentationName>APO-Sumatriptan</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sumatriptan succinate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/05/2011 09:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>160196-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sumatriptan (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>187210</Austr>
				<PresentationName>Sumatriptan (GA)</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>25/11/2013 12:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>187210-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sumatriptan (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>160186</Austr>
				<PresentationName>Sumatriptan generichealth</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>160186-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sumatriptan (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>154817</Austr>
				<PresentationName>Sumatriptan (Pharmacor)</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/08/2010 11:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154817-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sumatriptan (Ranbaxy)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>154819</Austr>
				<PresentationName>Sumatriptan RBX</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2013 09:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154819-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sumatriptan succinate (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>187214</Austr>
				<PresentationName>Sumatriptan Sandoz</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/12/2014 13:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>187214-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>187215</Austr>
				<PresentationName>Sumatriptan Sandoz</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/12/2014 13:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>187215-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Supradyn</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>117506</Austr>
				<PresentationName>Supradyn</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>tube</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2009 14:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow speckled</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>117506-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>117506-B01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Surgam</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>96238</Austr>
				<PresentationName>Surgam</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tiaprofenic acid</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/07/2008 13:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to creamy</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SURGAM 300</Side1Marking>
							<Side2Marking>logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96238-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Surmontil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>27562</Austr>
				<PresentationName>Surmontil</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Trimipramine maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/11/2008 13:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SURMONTIL 25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>27562-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>55559</Austr>
				<PresentationName>Surmontil</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Trimipramine maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/11/2008 13:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>SU 50</Side1Marking>
							<Side2Marking>SU 50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>55559-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Sutent</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>149114</Austr>
				<PresentationName>Sutent</PresentationName>
    			<PresentionStrength>12.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sunitinib malate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sutent</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>sunitinib malate</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/12/2019 14:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>Swedish orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Pfizer</Side1Marking>
							<Side2Marking>STN 12.5mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>149114-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>149115</Austr>
				<PresentationName>Sutent</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sunitinib malate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sutent</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>sunitinib malate</ActiveIngredient>
						<ReleaseDate>2019-11-06 08:26:50.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/12/2019 14:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>caramel and Swedish orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Pfizer</Side1Marking>
							<Side2Marking>STN 25mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>149115-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>149116</Austr>
				<PresentationName>Sutent</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sunitinib malate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Sutent</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>sunitinib malate</ActiveIngredient>
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				<Images>
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						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>caramel</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>Pfizer</Side1Marking>
							<Side2Marking>STN 50mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>149116-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Symmetrel</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>11057</Austr>
				<PresentationName>Symmetrel</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Amantadine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Symmetrel</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcsymor10420</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>amantadine hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-05-20 12:45:34.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2010 13:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>brown</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>GB</Side1Marking>
							<Side2Marking>GEIGY</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>11057-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Syquet</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>162401</Austr>
				<PresentationName>Syquet</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/06/2012 13:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>QTP</Side1Marking>
							<Side2Marking>25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>162401-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>162402</Austr>
				<PresentationName>Syquet</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/06/2012 13:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>QTP</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>162402-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>162404</Austr>
				<PresentationName>Syquet</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/06/2012 13:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>QTP</Side1Marking>
							<Side2Marking>200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>162404-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>162404-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>162405</Austr>
				<PresentationName>Syquet</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/06/2012 13:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>QTP</Side1Marking>
							<Side2Marking>300</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>162405-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>203592</Austr>
				<PresentationName>Syquet</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Syquet</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcsyque10218</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>quetiapine fumarate</ActiveIngredient>
						<ReleaseDate>2018-02-02 08:57:33.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/06/2019 06:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>203592-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>203593</Austr>
				<PresentationName>Syquet</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Syquet</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcsyque10218</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>quetiapine fumarate</ActiveIngredient>
						<ReleaseDate>2018-02-02 08:57:33.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/06/2019 06:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>203593-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>203593-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>203594</Austr>
				<PresentationName>Syquet</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Syquet</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcsyque10218</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>quetiapine fumarate</ActiveIngredient>
						<ReleaseDate>2018-02-02 08:57:33.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/06/2019 07:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>203594-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>204152</Austr>
				<PresentationName>Syquet</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Syquet</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcsyque10218</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>quetiapine fumarate</ActiveIngredient>
						<ReleaseDate>2018-02-02 08:57:33.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/12/2018 11:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>204152-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tacidine</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>94204</Austr>
				<PresentationName>Tacidine</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nizatidine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tacidine</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afctacid10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>nizatidine</ActiveIngredient>
						<ReleaseDate>2022-08-05 10:43:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>pale yellow and dark yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>G</Side1Marking>
							<Side2Marking>NZ 150</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>94204-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>94205</Austr>
				<PresentationName>Tacidine</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nizatidine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tacidine</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afctacid10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>nizatidine</ActiveIngredient>
						<ReleaseDate>2022-08-05 10:43:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light brown</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>G</Side1Marking>
							<Side2Marking>NZ 300</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>94205-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tacrograf</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167286</Austr>
				<PresentationName>Tacrograf</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/10/2018 14:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>SAL</Side1Marking>
							<Side2Marking>720</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167286-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>167288</Austr>
				<PresentationName>Tacrograf</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/10/2018 14:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>SAL</Side1Marking>
							<Side2Marking>721</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167288-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>167290</Austr>
				<PresentationName>Tacrograf</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/10/2018 14:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>teal opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>SAL</Side1Marking>
							<Side2Marking>722</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167290-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tacrolimus (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>209269</Austr>
				<PresentationName>Tacrolimus APOTEX</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>greyish-red</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>5.0 mg</Side1Marking>
							<Side2Marking>Tacro</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>209269-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>209273</Austr>
				<PresentationName>Tacrolimus APOTEX</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>0.5 mg</Side1Marking>
							<Side2Marking>Tacro</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>209273-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>209275</Austr>
				<PresentationName>Tacrolimus APOTEX</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>1.0 mg</Side1Marking>
							<Side2Marking>Tacro</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>209275-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tacrolimus (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>209266</Austr>
				<PresentationName>Pharmacor Tacrolimus</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2015 15:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>1.0mg</Side1Marking>
							<Side2Marking>Tacro</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>209266-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>209272</Austr>
				<PresentationName>Pharmacor Tacrolimus</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2015 15:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>0.5mg</Side1Marking>
							<Side2Marking>Tacro</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>209272-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tacrolimus (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>153744</Austr>
				<PresentationName>Tacrolimus Sandoz</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tacrolimus</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 13:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and ivory opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153744-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>153745</Austr>
				<PresentationName>Tacrolimus Sandoz</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tacrolimus</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 13:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and light brown opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153745-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>153746</Austr>
				<PresentationName>Tacrolimus Sandoz</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tacrolimus</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 13:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and orange opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153746-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>229738</Austr>
				<PresentationName>Tacrolimus Sandoz</PresentationName>
    			<PresentionStrength>0.75mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>tacrolimus monohydrate,lactose monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light green opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>0.75 mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>229738-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>229757</Austr>
				<PresentationName>Tacrolimus Sandoz</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>lactose monohydrate,tacrolimus monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>09/01/2018 16:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>dark green opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>2 mg</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>229757-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tadalafil (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>282075</Austr>
				<PresentationName>APO-Tadalafil </PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/02/2021 13:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>T5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>282075-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>282076</Austr>
				<PresentationName>APO-Tadalafil</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/02/2021 13:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>T10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>282076-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>282077</Austr>
				<PresentationName>APO-Tadalafil </PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/02/2021 13:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>T20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>282077-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tafinlar</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>200922</Austr>
				<PresentationName>Tafinlar</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Dabrafenib mesilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tafinlar</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvctafor10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>dabrafenib mesilate</ActiveIngredient>
						<ReleaseDate>2022-06-21 11:50:35.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>02/05/2016 17:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque dark red</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>GS TEW</Side1Marking>
							<Side2Marking>50 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>200922-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>200936</Austr>
				<PresentationName>Tafinlar</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Dabrafenib mesilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tafinlar</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvctafor10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>dabrafenib mesilate</ActiveIngredient>
						<ReleaseDate>2022-06-21 11:50:35.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>02/05/2016 17:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque dark pink</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>GS LHF</Side1Marking>
							<Side2Marking>75 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>200936-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tagrisso</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>255492</Austr>
				<PresentationName>Tagrisso</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>osimertinib mesilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tagrisso</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apctagri11122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>osimertinib mesilate</ActiveIngredient>
						<ReleaseDate>2022-11-08 14:27:33.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/04/2017 10:37</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>AZ 80</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>255492-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>255493</Austr>
				<PresentationName>Tagrisso</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>osimertinib mesilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tagrisso</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apctagri11122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>osimertinib mesilate</ActiveIngredient>
						<ReleaseDate>2022-11-08 14:27:33.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/04/2017 13:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>AZ 40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>255493-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Talam</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>212219</Austr>
				<PresentationName>Talam</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/08/2018 12:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C A</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>212219-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>212220</Austr>
				<PresentationName>Talam</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/08/2018 13:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>C A</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>212220-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>234594</Austr>
				<PresentationName>Talam</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/08/2018 13:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234594-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>234596</Austr>
				<PresentationName>Talam</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/08/2018 13:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>BL</Side1Marking>
							<Side2Marking>40</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>234596-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Talminex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>312887</Austr>
				<PresentationName>Talminex</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Talminex capsules</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afctalmx11122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>oseltamivir phosphate</ActiveIngredient>
						<ReleaseDate>2022-12-01 14:04:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/03/2022 12:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light yellow opaque and grey opaque, black band</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>75mg</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>312887-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tamate</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>150444</Austr>
				<PresentationName>Tamate</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Topiramate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tamate</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afctamat10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>topiramate</ActiveIngredient>
						<ReleaseDate>2022-07-11 16:05:32.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/02/2010 15:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TO 200</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>150444-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>150445</Austr>
				<PresentationName>Tamate</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Topiramate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tamate</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afctamat10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>topiramate</ActiveIngredient>
						<ReleaseDate>2022-07-11 16:05:32.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/02/2010 15:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TO 50</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>150445-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>150446</Austr>
				<PresentationName>Tamate</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Topiramate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tamate</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afctamat10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>topiramate</ActiveIngredient>
						<ReleaseDate>2022-07-11 16:05:32.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/02/2010 15:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TO 100</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>150446-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>150447</Austr>
				<PresentationName>Tamate</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Topiramate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tamate</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afctamat10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>topiramate</ActiveIngredient>
						<ReleaseDate>2022-07-11 16:05:32.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/02/2010 15:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TO 25</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>150447-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tambocor</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>41001</Austr>
				<PresentationName>Tambocor</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Flecainide acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tambocor</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>iactambo11121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>flecainide acetate</ActiveIngredient>
						<ReleaseDate>2021-12-03 14:30:03.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/09/2020 12:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TR 50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>41001-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>41002</Austr>
				<PresentationName>Tambocor</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Flecainide acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tambocor</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>iactambo11121</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>flecainide acetate</ActiveIngredient>
						<ReleaseDate>2021-12-03 14:30:03.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/11/2019 09:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TR 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>41002-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tamiflu</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>145953</Austr>
				<PresentationName>Tamiflu</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oseltamivir phosphate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tamiflu</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>roctamif20522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>oseltamivir phosphate</ActiveIngredient>
						<ReleaseDate>2022-05-30 14:18:35.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/11/2010 11:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light yellow opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>ROCHE</Side1Marking>
							<Side2Marking>30 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>145953-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>145957</Austr>
				<PresentationName>Tamiflu</PresentationName>
    			<PresentionStrength>45mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oseltamivir phosphate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tamiflu</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>roctamif20522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>oseltamivir phosphate</ActiveIngredient>
						<ReleaseDate>2022-05-30 14:18:35.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/11/2010 11:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>grey opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>ROCHE</Side1Marking>
							<Side2Marking>45 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>145957-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>76017</Austr>
				<PresentationName>Tamiflu</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oseltamivir phosphate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tamiflu</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>roctamif20522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>oseltamivir phosphate</ActiveIngredient>
						<ReleaseDate>2022-05-30 14:18:35.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/09/2008 13:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light yellow/opaque and grey/opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>ROCHE</Side1Marking>
							<Side2Marking>75 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>76017-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tamosin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>43527</Austr>
				<PresentationName>Tamosin</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>43527-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tamoxifen (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>145982</Austr>
				<PresentationName>Tamoxen</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 13:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>145982-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tamoxifen (GenRx)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>153122</Austr>
				<PresentationName>GenRx Tamoxifen</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/10/2010 11:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153122-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tamoxifen (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>80076</Austr>
				<PresentationName>Tamoxifen Sandoz</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tamoxifen citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>80076-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tamsil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167577</Austr>
				<PresentationName>Tamsil</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/10/2018 16:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>R250</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167577-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tamsulosin hydrochloride (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>313161</Austr>
				<PresentationName>APO-Tamsulosin SR</PresentationName>
    			<PresentionStrength>400mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/08/2021 16:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TSLN</Side1Marking>
							<Side2Marking>0.4</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>313161-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tamsulosin hydrochloride (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>196007</Austr>
				<PresentationName>Tamsulosin Sandoz SR</PresentationName>
    			<PresentionStrength>400mcg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tamsulosin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/04/2014 14:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>0.4</Side1Marking>
							<Side2Marking>SZ</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>196007-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tarceva</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>114714</Austr>
				<PresentationName>Tarceva</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Erlotinib hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tarceva</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>roctarce10319</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>erlotinib hydrochloride</ActiveIngredient>
						<ReleaseDate>2019-03-11 08:52:50.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/09/2008 16:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to yellowish</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TARCEVA 25 logo</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>114714-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>114717</Austr>
				<PresentationName>Tarceva</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Erlotinib hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tarceva</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>roctarce10319</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>erlotinib hydrochloride</ActiveIngredient>
						<ReleaseDate>2019-03-11 08:52:50.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/09/2008 16:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to yellowish</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TARCEVA 100 logo</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>114717-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>114721</Austr>
				<PresentationName>Tarceva</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Erlotinib hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tarceva</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>roctarce10319</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>erlotinib hydrochloride</ActiveIngredient>
						<ReleaseDate>2019-03-11 08:52:50.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/03/2015 11:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to yellowish</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>T 150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>114721-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Targin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>156067</Austr>
				<PresentationName>Targin</PresentationName>
    			<PresentionStrength>5mg/2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Naloxone hydrochloride,Oxycodone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>17/12/2010 14:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>OXN</Side1Marking>
							<Side2Marking>5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156067-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156145</Austr>
				<PresentationName>Targin</PresentationName>
    			<PresentionStrength>10mg/5mg </PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oxycodone hydrochloride,Naloxone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>17/12/2010 14:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>OXN</Side1Marking>
							<Side2Marking>10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156145-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156189</Austr>
				<PresentationName>Targin</PresentationName>
    			<PresentionStrength>20mg/10mg </PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Naloxone hydrochloride,Oxycodone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>17/12/2010 14:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>OXN</Side1Marking>
							<Side2Marking>20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156189-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>156194</Austr>
				<PresentationName>Targin</PresentationName>
    			<PresentionStrength>40mg/20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Naloxone hydrochloride,Oxycodone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>17/12/2010 14:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>OXN</Side1Marking>
							<Side2Marking>40</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156194-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216260</Austr>
				<PresentationName>Targin</PresentationName>
    			<PresentionStrength>2.5mg/1.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oxycodone hydrochloride,Naloxone hydrochloride anhydrous</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/11/2016 15:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216260-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216261</Austr>
				<PresentationName>Targin</PresentationName>
    			<PresentionStrength>15mg/7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Naloxone hydrochloride anhydrous,Oxycodone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/11/2016 15:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>grey</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>OXN</Side1Marking>
							<Side2Marking>15</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216261-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>216280</Austr>
				<PresentationName>Targin</PresentationName>
    			<PresentionStrength>30mg/15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oxycodone hydrochloride,Naloxone hydrochloride anhydrous</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/11/2016 15:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>OXN</Side1Marking>
							<Side2Marking>30</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>216280-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>243252</Austr>
				<PresentationName>Targin</PresentationName>
    			<PresentionStrength>60mg/30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>naloxone hydrochloride dihydrate,oxycodone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/06/2017 15:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>OXN</Side1Marking>
							<Side2Marking>60</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>243252-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>243272</Austr>
				<PresentationName>Targin</PresentationName>
    			<PresentionStrength>80mg/40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>oxycodone hydrochloride,naloxone hydrochloride dihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/06/2017 15:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>OXN</Side1Marking>
							<Side2Marking>80</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>243272-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tarka</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>104663</Austr>
				<PresentationName>Tarka</PresentationName>
    			<PresentionStrength>2mg/180mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Trandolapril,Verapamil hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tarka</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goctarka11221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>trandolapril with verapamil hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-12-07 16:00:46.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/04/2021 13:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>182</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>104663-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>104664</Austr>
				<PresentationName>Tarka</PresentationName>
    			<PresentionStrength>4mg/240mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Verapamil hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tarka</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goctarka11221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>trandolapril with verapamil hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-12-07 16:00:46.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/04/2018 13:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red-brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>244</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>104664-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tasigna</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>133086</Austr>
				<PresentationName>Tasigna</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nilotinib hydrochloride monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tasigna</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvctasor11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>nilotinib</ActiveIngredient>
						<ReleaseDate>2022-10-26 08:35:05.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/12/2008 10:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light yellow opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>NVR</Side1Marking>
							<Side2Marking>TKI</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133086-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>171498</Austr>
				<PresentationName>Tasigna</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nilotinib</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tasigna</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvctasor11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>nilotinib</ActiveIngredient>
						<ReleaseDate>2022-10-26 08:35:05.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/11/2011 12:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>NVR</Side1Marking>
							<Side2Marking>BCR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>171498-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tazac</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>49325</Austr>
				<PresentationName>Tazac</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nizatidine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/11/2008 13:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light yellow and dark yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>N150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>49325-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>49326</Austr>
				<PresentationName>Tazac</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Nizatidine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/11/2008 13:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light yellow and brown</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>N300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>49326-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tegretol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>41846</Austr>
				<PresentationName>Tegretol</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Carbamazepine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tegretol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvctgror21020</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>carbamazepine</ActiveIngredient>
						<ReleaseDate>2022-11-03 15:17:40.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/09/2008 13:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>B W</Side1Marking>
							<Side2Marking>GEIGY</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>41846-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>41848</Austr>
				<PresentationName>Tegretol</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Carbamazepine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tegretol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvctgror21020</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>carbamazepine</ActiveIngredient>
						<ReleaseDate>2022-11-03 15:17:40.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/09/2008 13:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>G K</Side1Marking>
							<Side2Marking>CG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>41848-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>42944</Austr>
				<PresentationName>Tegretol CR</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Carbamazepine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tegretol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvctgror21020</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>carbamazepine</ActiveIngredient>
						<ReleaseDate>2022-11-03 15:17:40.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/09/2008 13:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown-orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>ENE ENE</Side1Marking>
							<Side2Marking>CG CG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>42944-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>42974</Austr>
				<PresentationName>Tegretol CR</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Carbamazepine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tegretol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvctgror21020</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>carbamazepine</ActiveIngredient>
						<ReleaseDate>2022-11-03 15:17:40.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2010 13:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige-orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>H C</Side1Marking>
							<Side2Marking>C G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>42974-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Telfast</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>63338</Austr>
				<PresentationName>Telfast</PresentationName>
    			<PresentionStrength>180mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>fexofenadine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Telfast</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swctelfa11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fexofenadine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-19 15:59:06.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/06/2008 15:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>018</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>63338-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>63339</Austr>
				<PresentationName>Telfast</PresentationName>
    			<PresentionStrength>120mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>fexofenadine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Telfast</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swctelfa11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fexofenadine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-19 15:59:06.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/06/2008 15:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>012</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>63339-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>70949</Austr>
				<PresentationName>Telfast</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>fexofenadine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Telfast</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swctelfa11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fexofenadine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-10-19 15:59:06.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/06/2008 15:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>06</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>70949-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>72552</Austr>
				<PresentationName>Telfast Decongestant</PresentationName>
    			<PresentionStrength>60/120mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>pseudoephedrine hydrochloride,fexofenadine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Telfast Decongestant</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swctelfd11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fexofenadine hydrochloride with pseudoephedrine hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-10-13 09:49:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/06/2008 15:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white and tan</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>06/012D</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>72552-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>75139</Austr>
				<PresentationName>Telfast 30mg</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>fexofenadine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Telfast Childrens Elixir and 30mg tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swctelfx10521</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fexofenadine hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-07-22 14:39:03.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/06/2008 15:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>03</Side1Marking>
							<Side2Marking>e</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75139-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Telmisartan (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>209335</Austr>
				<PresentationName>Telmisartan AN</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/10/2017 13:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L203</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>209335-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>209339</Austr>
				<PresentationName>Telmisartan AN</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/10/2017 13:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L204</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>209339-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Telmisartan (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>209334</Austr>
				<PresentationName>APO-Telmisartan</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Telmisartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L204</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>209334-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>209336</Austr>
				<PresentationName>APO-Telmisartan</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Telmisartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L203</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>209336-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Telmisartan (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>209337</Austr>
				<PresentationName>Telmisartan GH</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/05/2017 15:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L203</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>209337-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>209338</Austr>
				<PresentationName>Telmisartan GH</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/05/2017 15:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L204</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>209338-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Telmisartan (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>211905</Austr>
				<PresentationName>Pharmacor Telmisartan</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/01/2016 10:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>TEL</Side1Marking>
							<Side2Marking>40</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>211905-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>211909</Austr>
				<PresentationName>Pharmacor Telmisartan</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/01/2016 10:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>TEL</Side1Marking>
							<Side2Marking>80</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>211909-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Telmisartan (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>199698</Austr>
				<PresentationName>Telmisartan Sandoz</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Telmisartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/07/2016 11:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>80</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199698-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199699</Austr>
				<PresentationName>Telmisartan Sandoz</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Telmisartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/07/2016 11:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199699-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Telmisartan/HCT (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>208070</Austr>
				<PresentationName>Telmisartan HCT GH 40/12.5</PresentationName>
    			<PresentionStrength>40mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/05/2017 16:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled and white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L199</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>208070-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>208075</Austr>
				<PresentationName>Telmisartan HCT GH 80/12.5</PresentationName>
    			<PresentionStrength>80mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/05/2017 16:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled and white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>208075-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>208076</Austr>
				<PresentationName>Telmisartan HCT GH 80/25</PresentationName>
    			<PresentionStrength>80mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/05/2017 16:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow mottled and white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L201</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>208076-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Telmisartan/HCT (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>201356</Austr>
				<PresentationName>Telmisartan/HCT Sandoz</PresentationName>
    			<PresentionStrength>40mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Telmisartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/07/2016 11:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>40</Side1Marking>
							<Side2Marking>12.5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>201356-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>201358</Austr>
				<PresentationName>Telmisartan/HCT Sandoz</PresentationName>
    			<PresentionStrength>80mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Telmisartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/07/2016 11:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>80</Side1Marking>
							<Side2Marking>25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>201358-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>201359</Austr>
				<PresentationName>Telmisartan/HCT Sandoz</PresentationName>
    			<PresentionStrength>80mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Telmisartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/07/2016 11:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>80</Side1Marking>
							<Side2Marking>12.5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>201359-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Telmisartan/HCTZ (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>221179</Austr>
				<PresentationName>Telmisartan HCTZ AN</PresentationName>
    			<PresentionStrength>40mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/10/2017 13:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled and white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L199</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>221179-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>221180</Austr>
				<PresentationName>Telmisartan HCTZ AN</PresentationName>
    			<PresentionStrength>80mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/10/2017 13:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled and white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>221180-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>221181</Austr>
				<PresentationName>Telmisartan HCTZ AN</PresentationName>
    			<PresentionStrength>80mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/10/2017 13:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow mottled and white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L201</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>221181-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Telmisartan/HCTZ (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>208063</Austr>
				<PresentationName>APO-Telmisartan HCTZ</PresentationName>
    			<PresentionStrength>80mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>hydrochlorothiazide,telmisartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow mottled and white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L201</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>208063-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>208064</Austr>
				<PresentationName>APO-Telmisartan HCTZ</PresentationName>
    			<PresentionStrength>40mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>telmisartan,hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled and white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L199</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>208064-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>208069</Austr>
				<PresentationName>APO-Telmisartan HCTZ</PresentationName>
    			<PresentionStrength>80mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>hydrochlorothiazide,telmisartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled and white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>208069-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Teltartan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>209341</Austr>
				<PresentationName>Teltartan</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/10/2018 16:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L203</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>209341-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>209343</Austr>
				<PresentationName>Teltartan</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/10/2018 16:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L204</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>209343-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Teltartan HCT</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>208067</Austr>
				<PresentationName>Teltartan HCT</PresentationName>
    			<PresentionStrength>80mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/10/2018 14:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled and white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>208067-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>208068</Austr>
				<PresentationName>Teltartan HCT</PresentationName>
    			<PresentionStrength>40mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/10/2018 14:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink mottled and white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L199</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>208068-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>208074</Austr>
				<PresentationName>Teltartan HCT</PresentationName>
    			<PresentionStrength>80mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/10/2018 16:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow mottled and white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>L201</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>208074-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Telzir</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>101604</Austr>
				<PresentationName>Telzir Tablets</PresentationName>
    			<PresentionStrength>700mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Fosamprenavir calcium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Telzir Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>victelzr10918</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fosamprenavir calcium</ActiveIngredient>
						<ReleaseDate>2018-12-17 13:52:39.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 15:32</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>GXLL7</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101604-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Temaze</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>63863</Austr>
				<PresentationName>Temaze</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Temazepam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Temaze</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afctemaz11120</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>temazepam</ActiveIngredient>
						<ReleaseDate>2020-11-24 10:25:48.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TE 10</Side1Marking>
							<Side2Marking>&#945;</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>63863-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Temazepam (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>153123</Austr>
				<PresentationName>Apo-Temazepam</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/05/2010 09:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>S</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153123-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Temgesic</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>34091</Austr>
				<PresentationName>Temgesic</PresentationName>
    			<PresentionStrength>200mcg</PresentionStrength>
    			<PresentationForm>Sublingual Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Buprenorphine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/02/2017 11:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>L</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>34091-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Temodal</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>164210</Austr>
				<PresentationName>Temodal</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>sachet</Container>
    			<TGAIngredient>Temozolomide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Temodal</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>mkctemod20222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>temozolomide</ActiveIngredient>
						<ReleaseDate>2022-03-11 17:30:44.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>18/07/2012 16:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TEMODAL</Side1Marking>
							<Side2Marking>5 mg Schering-Plough Logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>164210-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>164211</Austr>
				<PresentationName>Temodal</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>sachet</Container>
    			<TGAIngredient>Temozolomide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Temodal</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>mkctemod20222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>temozolomide</ActiveIngredient>
						<ReleaseDate>2022-03-11 17:30:44.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>18/07/2012 16:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TEMODAL</Side1Marking>
							<Side2Marking>20 mg Schering-Plough Logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>164211-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>164212</Austr>
				<PresentationName>Temodal</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>sachet</Container>
    			<TGAIngredient>Temozolomide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Temodal</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>mkctemod20222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>temozolomide</ActiveIngredient>
						<ReleaseDate>2022-03-11 17:30:44.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>18/07/2012 16:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and pink</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TEMODAL</Side1Marking>
							<Side2Marking>100 mg Schering-Plough Logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>164212-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
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			<Presentations>
				<Austr>164213</Austr>
				<PresentationName>Temodal</PresentationName>
    			<PresentionStrength>140mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>sachet</Container>
    			<TGAIngredient>Temozolomide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Temodal</DocumentName>
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								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>temozolomide</ActiveIngredient>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>29/02/2012 14:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TEMODAL</Side1Marking>
							<Side2Marking>140 mg Schering-Plough Logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>164213-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>164215</Austr>
				<PresentationName>Temodal</PresentationName>
    			<PresentionStrength>180mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>sachet</Container>
    			<TGAIngredient>Temozolomide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Temodal</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>temozolomide</ActiveIngredient>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/08/2013 09:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TEMODAL</Side1Marking>
							<Side2Marking>180 mg Schering Plough Logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>164216</Austr>
				<PresentationName>Temodal</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>sachet</Container>
    			<TGAIngredient>Temozolomide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Temodal</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>temozolomide</ActiveIngredient>
						<ReleaseDate>2022-03-11 17:30:44.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>18/07/2012 16:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TEMODAL</Side1Marking>
							<Side2Marking>250 mg Schering-Plough Logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>164216-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>68720</Austr>
				<PresentationName>Temodal</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Temozolomide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>05/01/2011 16:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TEMODAL</Side1Marking>
							<Side2Marking>250 mg Schering-Plough Logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>68720-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>68721</Austr>
				<PresentationName>Temodal</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Temozolomide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>05/01/2011 16:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and pink</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TEMODAL</Side1Marking>
							<Side2Marking>100 mg Schering-Plough Logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>68721-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>68722</Austr>
				<PresentationName>Temodal</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Temozolomide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TEMODAL</Side1Marking>
							<Side2Marking>20 mg Schering-Plough Logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>68722-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>68723</Austr>
				<PresentationName>Temodal</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Temozolomide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>07/11/2011 13:48</DateEffective>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and green</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TEMODAL</Side1Marking>
							<Side2Marking>5 mg Schering-Plough Logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>68723-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Temozolomide (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>192683</Austr>
				<PresentationName>Temozolomide AN</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>26/07/2017 16:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>buff</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TMZ</Side1Marking>
							<Side2Marking>250 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192683-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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			</Presentations>
			<Presentations>
				<Austr>192689</Austr>
				<PresentationName>Temozolomide AN</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>flesh</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TMZ</Side1Marking>
							<Side2Marking>100 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192689-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>192691</Austr>
				<PresentationName>Temozolomide AN</PresentationName>
    			<PresentionStrength>140mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>powder blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TMZ</Side1Marking>
							<Side2Marking>140 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192691-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>192693</Austr>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light green opaque</Colour>
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							<Shape></Shape>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192693-C01-01-BL600.jpg</ImageFileName>
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			<Presentations>
				<Austr>192694</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
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							<PhaseItem>1</PhaseItem>
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							<Colour>rich yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192694-C01-01-BL600.jpg</ImageFileName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
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					<Versions>
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							<PhaseItem>1</PhaseItem>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			<Presentations>
				<Austr>231524</Austr>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
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							<Colour>rich yellow opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>231524-C01-01-BL600.jpg</ImageFileName>
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			<Presentations>
				<Austr>231525</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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							<PhaseItem>1</PhaseItem>
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							<Colour>medium orange opaque</Colour>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			<Presentations>
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    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>buff opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TMZ</Side1Marking>
							<Side2Marking>250 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>231526-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>231527</Austr>
				<PresentationName>APO-Temozolomide</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Temozolomide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>flesh opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TMZ</Side1Marking>
							<Side2Marking>100 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>231527-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>231528</Austr>
				<PresentationName>APO-Temozolomide</PresentationName>
    			<PresentionStrength>140mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Temozolomide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/05/2016 20:30</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>powder blue opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TMZ</Side1Marking>
							<Side2Marking>140 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>231528-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Temtabs</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>91058</Austr>
				<PresentationName>Temtabs</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>S</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>91058-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tenofovir (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>247314</Austr>
				<PresentationName>Tenofovir Apotex</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tenofovir disoproxil fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/09/2018 09:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>almond-shaped</Shape>
							<Side1Marking>TEN 300</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>247314-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tenofovir Disoproxil (Viatris)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>261093</Austr>
				<PresentationName>Tenofovir Disoproxil Viatris</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>tenofovir disoproxil maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tenofovir Disoproxil Viatris</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afctenom10922</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tenofovir disoproxil maleate</ActiveIngredient>
						<ReleaseDate>2022-09-23 13:27:08.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/12/2018 10:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TM 300</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>261093-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>261093-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tenofovir Disoproxil Emtricitabine (Viatris)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>265834</Austr>
				<PresentationName>Tenofovir Disoproxil Emtricitabine Viatris</PresentationName>
    			<PresentionStrength>300mg/200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Emtricitabine,tenofovir disoproxil maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tenofovir Disoproxil Emtricitabine Viatris</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afctenoe10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tenofovir disoproxil maleate with emtricitabine</ActiveIngredient>
						<ReleaseDate>2022-09-02 10:38:54.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/12/2018 10:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>ETM</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>265834-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tenofovir Disoproxil Emtricitabine Efavirenz (Viatris)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>280721</Austr>
				<PresentationName>Tenofovir Disoproxil Emtricitabine Efavirenz Viatris</PresentationName>
    			<PresentionStrength>300mg/200mg/600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Efavirenz,tenofovir disoproxil maleate,Emtricitabine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tenofovir Disoproxil Emtricitabine Efavirenz Viatris</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afctdeem20422</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tenofovir disoproxil maleate with emtricitabine and efavirenz</ActiveIngredient>
						<ReleaseDate>2022-05-02 10:11:40.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/10/2019 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>TEE</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>280721-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tenofovir Disoproxil Fumarate with Emtricitabine (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>275070</Austr>
				<PresentationName>Tenofovir/Emtricitabine Apotex</PresentationName>
    			<PresentionStrength>300mg/200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Emtricitabine,Tenofovir disoproxil fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/11/2018 19:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>E-T</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>275070-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tenormin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>287200</Austr>
				<PresentationName>Tenormin</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atenolol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tenormin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>iyctenor10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>atenolol</ActiveIngredient>
						<ReleaseDate>2022-06-14 15:29:51.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/06/2018 10:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>287200-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tensig</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>147638</Austr>
				<PresentationName>Tensig</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
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						<DateEffective>26/08/2020 15:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>147638-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>77503</Austr>
				<PresentationName>Tensig</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/08/2020 15:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>77503-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tensodeine</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>138543</Austr>
				<PresentationName>Tensodeine</PresentationName>
    			<PresentionStrength>450mg/9.75mg/5mg</PresentionStrength>
    			<PresentationForm>Caplets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 19:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Caplets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>138543-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Terbinafine (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>100025</Austr>
				<PresentationName>APO-Terbinafine</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>terbinafine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/09/2008 13:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TER 250</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>100025-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Terbinafine (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>119754</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient></TGAIngredient>
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						<DateEffective>23/02/2009 13:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TER 250</Side1Marking>
							<Side2Marking>APO</Side2Marking>
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								<ViewLabel>C</ViewLabel>
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			</Presentations>
		</Brand><Brand>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>200224</Austr>
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    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>23/06/2015 16:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>200224-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Terbinafine (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>101685</Austr>
				<PresentationName>Terbinafine Sandoz</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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					<Versions>
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						<DateEffective>29/04/2011 15:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to almost white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TER 250</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>101685-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
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			</Presentations>
		</Brand><Brand>
			<brandname>Teriflagio</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>303521</Austr>
				<PresentationName>Teriflagio</PresentationName>
    			<PresentionStrength>14mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/06/2020 11:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>pentagonal</Shape>
							<Side1Marking>T2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>303521-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Teriflunomide (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>304232</Austr>
				<PresentationName>APO-Teriflunomide</PresentationName>
    			<PresentionStrength>14mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/03/2020 20:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale blue to pastel blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>pentagonal</Shape>
							<Side1Marking>T</Side1Marking>
							<Side2Marking>14</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>304232-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
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			</Presentations>
		</Brand><Brand>
			<brandname>Terimide</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>299149</Austr>
				<PresentationName>Terimide</PresentationName>
    			<PresentionStrength>14mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>teriflunomide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Terimide</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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							<PhaseItem>1</PhaseItem>
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							<Colour>pale blue to pastel blue</Colour>
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							<Shape>pentagonal</Shape>
							<Side1Marking>598</Side1Marking>
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								<ViewLabel>C</ViewLabel>
								<ImageFileName>299149-C01-01-BL600.jpg</ImageFileName>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>13695</Austr>
				<PresentationName>Tetrabenazine</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
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    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<Colour>buff</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CL 25</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>13695-C01-01-BL600.jpg</ImageFileName>
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		</Brand><Brand>
			<brandname>Tevaripiprazole</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>238013</Austr>
				<PresentationName>Tevaripiprazole </PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-09 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>21/11/2018 16:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>238013-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>238014</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-09 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>aripiprazole</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
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							<Colour>pink to light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>10</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>238014-C01-01-BL600.jpg</ImageFileName>
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			<Presentations>
				<Austr>238032</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-09 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>15</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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								<ViewLabel>C</ViewLabel>
								<ImageFileName>238032-C01-01-BL600.jpg</ImageFileName>
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			<Presentations>
				<Austr>238033</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
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    			<TGAIngredient>aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>238033-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>238034</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-08-09 00:00:00'}</WithdrawalDate>
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    			<TGAIngredient>aripiprazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>21/11/2018 16:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink to light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>30</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>238034-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>249712</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/02/2018 16:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>Q50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>249712-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
				<Austr>249752</Austr>
				<PresentationName>Tevatiapine XR</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tevatiapine XR</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>quetiapine fumarate</ActiveIngredient>
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				<Images>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>Q150</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>249752-C01-01-BL600.jpg</ImageFileName>
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			<Presentations>
				<Austr>249772</Austr>
				<PresentationName>Tevatiapine XR</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tevatiapine XR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcquexr10122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>quetiapine fumarate</ActiveIngredient>
						<ReleaseDate>2022-01-25 11:09:47.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/02/2018 16:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>Q200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>249772-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>249792</Austr>
				<PresentationName>Tevatiapine XR</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tevatiapine XR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tbcquexr10122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>quetiapine fumarate</ActiveIngredient>
						<ReleaseDate>2022-01-25 11:09:47.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/02/2018 16:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>Q300</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>249792-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>249812</Austr>
				<PresentationName>Tevatiapine XR</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Quetiapine fumarate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tevatiapine XR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>quetiapine fumarate</ActiveIngredient>
						<ReleaseDate>2022-01-25 11:09:47.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/02/2018 16:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>Q400</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>249812-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Teveten</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>64400</Austr>
				<PresentationName>Teveten</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Eprosartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Teveten</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goctevet10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>eprosartan mesilate</ActiveIngredient>
						<ReleaseDate>2022-02-11 13:36:40.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/01/2013 16:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>5044</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>64400-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>73779</Austr>
				<PresentationName>Teveten</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Eprosartan mesylate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Teveten</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goctevet10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>eprosartan mesilate</ActiveIngredient>
						<ReleaseDate>2022-02-11 13:36:40.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/01/2013 16:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>5046</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73779-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Teveten Plus</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>143172</Austr>
				<PresentationName>Teveten Plus</PresentationName>
    			<PresentionStrength>600mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Eprosartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Teveten Plus</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
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					</DocumentQualifiers>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/01/2013 16:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>butterscotch</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>5147</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>143172-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Thioprine</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>221962</Austr>
				<PresentationName>Thioprine</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Thioprine 50</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcthior10220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>azathioprine</ActiveIngredient>
						<ReleaseDate>2020-02-12 10:06:50.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/03/2022 12:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to yellowish white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>221962-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tibolone (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>283952</Austr>
				<PresentationName>APO-Tibolone</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/02/2021 13:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TO 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>283952-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tinasil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>104493</Austr>
				<PresentationName>Tinasil</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Terbinafine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tinasil</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
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					</DocumentQualifiers>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/07/2011 13:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TF 250</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>104493-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tivicay</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>205212</Austr>
				<PresentationName>Tivicay</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Dolutegravir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tivicay</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>dolutegravir</ActiveIngredient>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/09/2016 09:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SV 572</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>205212-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>312781</Austr>
				<PresentationName>Tivicay</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>dolutegravir sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tivicay</DocumentName>
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							<AvailableFormats>
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						<ActiveIngredient>dolutegravir</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/07/2020 12:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SV 572</Side1Marking>
							<Side2Marking>25</Side2Marking>
							<Views>
							<View>
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								<ImageFileName>312781-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>312782</Austr>
				<PresentationName>Tivicay</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>dolutegravir sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tivicay</DocumentName>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/07/2020 12:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SV 572</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>312782-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tixol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>199256</Austr>
				<PresentationName>Tixol</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Duloxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tixol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afctixol11220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>duloxetine hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-12-08 13:51:00.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/12/2018 16:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>157</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199256-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199265</Austr>
				<PresentationName>Tixol</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Duloxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tixol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afctixol11220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>duloxetine hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-12-08 13:51:00.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/07/2019 08:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue and green opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>A</Side1Marking>
							<Side2Marking>158</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199265-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tobi</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>182302</Austr>
				<PresentationName>Tobi Podhaler</PresentationName>
    			<PresentionStrength>28mg</PresentionStrength>
    			<PresentationForm>Inhalation Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tobramycin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tobi Podhaler</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goctobip11221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tobramycin</ActiveIngredient>
						<ReleaseDate>2021-12-09 16:46:34.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>02/05/2016 17:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>clear colourless</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>NVR AVCI</Side1Marking>
							<Side2Marking>Novartis logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>182302-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tofranil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>11064</Austr>
				<PresentationName>Tofranil</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Imipramine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tofranil</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ghcimipr11117</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>imipramine hydrochloride</ActiveIngredient>
						<ReleaseDate>2018-11-14 15:31:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/02/2020 16:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red-brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>triangular</Shape>
							<Side1Marking>FT</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>11064-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>60673</Austr>
				<PresentationName>Tofranil</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Imipramine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tofranil</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ghcimipr11117</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>imipramine hydrochloride</ActiveIngredient>
						<ReleaseDate>2018-11-14 15:31:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/02/2020 16:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish-brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CZ</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>60673-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tolerade</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>117785</Austr>
				<PresentationName>Tolerade</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/11/2008 13:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish-brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>triangular</Shape>
							<Side1Marking>F T</Side1Marking>
							<Side2Marking>C G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>117785-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>117786</Austr>
				<PresentationName>Tolerade</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/11/2008 13:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish-brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>C Z</Side1Marking>
							<Side2Marking>C G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>117786-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tolvon</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>65541</Austr>
				<PresentationName>Tolvon</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mianserin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/10/2010 11:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CT 4</Side1Marking>
							<Side2Marking>ORGANON *</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>65541-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>65543</Austr>
				<PresentationName>Tolvon</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Mianserin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>18/10/2010 11:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CT 6</Side1Marking>
							<Side2Marking>ORGANON *</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>65543-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Topamax</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>167729</Austr>
				<PresentationName>Topamax</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Sprinkle Caps.</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Topamax</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jcctopam10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>topiramate</ActiveIngredient>
						<ReleaseDate>2022-05-31 14:26:39.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/07/2010 16:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Sprinkle Caps.</DoseForm>
							<Colour>clear and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TOP</Side1Marking>
							<Side2Marking>15 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167729-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>167730</Austr>
				<PresentationName>Topamax</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Sprinkle Caps.</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Topamax</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jcctopam10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>topiramate</ActiveIngredient>
						<ReleaseDate>2022-05-31 14:26:39.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/07/2010 16:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Sprinkle Caps.</DoseForm>
							<Colour>clear and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TOP</Side1Marking>
							<Side2Marking>25 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167730-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>167731</Austr>
				<PresentationName>Topamax</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Sprinkle Caps</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Topamax</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jcctopam10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>topiramate</ActiveIngredient>
						<ReleaseDate>2022-05-31 14:26:39.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/07/2010 16:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Sprinkle Caps</DoseForm>
							<Colour>clear and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TOP</Side1Marking>
							<Side2Marking>50 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>167731-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>62709</Austr>
				<PresentationName>Topamax</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Topamax</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jcctopam10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>topiramate</ActiveIngredient>
						<ReleaseDate>2022-05-31 14:26:39.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/07/2008 09:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TOP</Side1Marking>
							<Side2Marking>25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62709-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>62710</Austr>
				<PresentationName>Topamax</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Topamax</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jcctopam10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>topiramate</ActiveIngredient>
						<ReleaseDate>2022-05-31 14:26:39.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/07/2008 09:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TOP</Side1Marking>
							<Side2Marking>50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62710-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>62711</Austr>
				<PresentationName>Topamax</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Topamax</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jcctopam10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>topiramate</ActiveIngredient>
						<ReleaseDate>2022-05-31 14:26:39.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/07/2008 09:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TOP</Side1Marking>
							<Side2Marking>100</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62711-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>62712</Austr>
				<PresentationName>Topamax</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Topamax</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>jcctopam10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>topiramate</ActiveIngredient>
						<ReleaseDate>2022-05-31 14:26:39.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/07/2008 09:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>salmon</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TOP</Side1Marking>
							<Side2Marking>200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>62712-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Topiramate (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>124729</Austr>
				<PresentationName>APO-Topiramate</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Topiramate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/05/2010 09:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TP 25</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>124729-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>124730</Austr>
				<PresentationName>APO-Topiramate</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Topiramate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/05/2010 09:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TP 50</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>124730-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>124731</Austr>
				<PresentationName>APO-Topiramate</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Topiramate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/05/2010 09:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>mustard yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TP 100</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>124731-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>124732</Austr>
				<PresentationName>APO-Topiramate</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Topiramate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/05/2010 09:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish-brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TP 200</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>124732-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Topiramate (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>135766</Austr>
				<PresentationName>Topiramate GH</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/05/2017 17:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135766-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>135790</Austr>
				<PresentationName>Topiramate GH</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/05/2017 17:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135790-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>135797</Austr>
				<PresentationName>Topiramate GH</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/05/2017 17:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135797-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>135815</Austr>
				<PresentationName>Topiramate GH</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/05/2017 17:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135815-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Topiramate (Ranbaxy)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>157964</Austr>
				<PresentationName>RBX Topiramate</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/10/2010 09:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>TP1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157964-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>157966</Austr>
				<PresentationName>RBX Topiramate</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/10/2010 09:31</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>TP3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157966-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>157971</Austr>
				<PresentationName>RBX Topiramate</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/10/2010 09:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>TP2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157971-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>157973</Austr>
				<PresentationName>RBX Topiramate</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/10/2010 09:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>TP4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>157973-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Topiramate (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>135762</Austr>
				<PresentationName>Topiramate Sandoz</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Topiramate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>135779</Austr>
				<PresentationName>Topiramate Sandoz</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Topiramate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>28/05/2012 13:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>135794</Austr>
				<PresentationName>Topiramate Sandoz</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Topiramate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>28/05/2012 13:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>135794-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>135810</Austr>
				<PresentationName>Topiramate Sandoz</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Topiramate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/05/2012 13:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>135810-A01-01-BL600.jpg</ImageFileName>
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							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>135810-B01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Toprol-XL</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>115007</Austr>
				<PresentationName>Toprol-XL Titration Pack</PresentationName>
    			<PresentionStrength></PresentionStrength>
    			<PresentationForm>Combination Pack</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>Yes</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/07/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>None</DoseForm>
							<Colour></Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
								<View></View>
								<ImageFileName />
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>97785</Austr>
				<PresentationName>Toprol-XL</PresentationName>
    			<PresentionStrength>23.75mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metoprolol succinate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR>115007</IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<QualiferData></QualiferData>
						<DocumentName>Toprol-XL</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>metoprolol succinate</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 11:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>A ß</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>97785-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>97786</Austr>
				<PresentationName>Toprol-XL</PresentationName>
    			<PresentionStrength>47.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metoprolol succinate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR>115007</IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Toprol-XL</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>metoprolol succinate</ActiveIngredient>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/08/2008 11:15</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>A MO</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>97787</Austr>
				<PresentationName>Toprol-XL</PresentationName>
    			<PresentionStrength>95mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metoprolol succinate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR>115007</IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Toprol-XL</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
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						</DocumentTypes>
						<ActiveIngredient>metoprolol succinate</ActiveIngredient>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>A MS</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>97788</Austr>
				<PresentationName>Toprol-XL</PresentationName>
    			<PresentionStrength>190mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metoprolol succinate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Toprol-XL</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
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						<ActiveIngredient>metoprolol succinate</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>A MY</Side1Marking>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Toradol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>42060</Austr>
				<PresentationName>Toradol</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ketorolac trometamol</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<QualiferData></QualiferData>
						<DocumentName>Toradol Tablets</DocumentName>
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							<AvailableFormats>
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						<ActiveIngredient>ketorolac trometamol</ActiveIngredient>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to creamy white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>KET 10</Side1Marking>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Torvastat</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>194111</Austr>
				<PresentationName>Torvastat</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>22/10/2018 14:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>A</Side1Marking>
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							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>194113</Austr>
				<PresentationName>Torvastat</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
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							<Side1Marking>A</Side1Marking>
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							<Views>
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			<Presentations>
				<Austr>194115</Austr>
				<PresentationName>Torvastat</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<brandname>Tracleer</brandname>
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			<Presentations>
				<Austr>91919</Austr>
				<PresentationName>Tracleer</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>bosentan monohydrate</TGAIngredient>
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			<Presentations>
				<Austr>91920</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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							<Views>
							<View>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trajenta</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>175499</Austr>
				<PresentationName>Trajenta</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
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								<Format>PDF</Format>
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						<DateEffective>19/01/2012 10:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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								<ViewLabel>C</ViewLabel>
								<ImageFileName>175499-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trajentamet</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>195088</Austr>
				<PresentationName>Trajentamet</PresentationName>
    			<PresentionStrength>2.5mg/500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>metformin hydrochloride,linagliptin</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Trajentamet</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>linagliptin with metformin hydrochloride</ActiveIngredient>
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					<Versions>
						<VersionSequence>2</VersionSequence>
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						<DateEffective>22/10/2015 12:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>D2/500</Side1Marking>
							<Side2Marking>Boehringer Ingelheim logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195088-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>195101</Austr>
				<PresentationName>Trajentamet</PresentationName>
    			<PresentionStrength>2.5mg/850mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>metformin hydrochloride,linagliptin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Trajentamet</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>linagliptin with metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-08-25 12:15:21.0</ReleaseDate>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/07/2014 11:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>D2/850</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195101-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>195107</Austr>
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    			<PresentionStrength>2.5mg/1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>metformin hydrochloride,linagliptin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Trajentamet</DocumentName>
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							<DocumentType>eCMI</DocumentType>
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								<Format>PDF</Format>
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						<ActiveIngredient>linagliptin with metformin hydrochloride</ActiveIngredient>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>17/07/2014 11:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>D2/1000</Side1Marking>
							<Side2Marking>Boehringer Ingelheim logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>195107-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tramadol Hydrochloride (Actavis)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>218122</Austr>
				<PresentationName>Tramadol Actavis</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>10/12/2014 15:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
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							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>218122-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tramadol Hydrochloride (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>190050</Austr>
				<PresentationName>Tramadol AN</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>13/10/2017 13:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>190050-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>190051</Austr>
				<PresentationName>Tramadol AN SR</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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								<ImageFileName>190051-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>190053</Austr>
				<PresentationName>Tramadol AN SR</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tramadol Hydrochloride (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>154393</Austr>
				<PresentationName>Apo-Tramadol SR</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/11/2011 16:01</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>154394</Austr>
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    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/11/2011 16:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154394-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>154395</Austr>
				<PresentationName>Apo-Tramadol SR</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/11/2011 15:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154395-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158470</Austr>
				<PresentationName>APO-Tramadol</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tramadol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/01/2012 15:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green and yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158470-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tramadol Hydrochloride (Chemmart)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>154396</Austr>
				<PresentationName>Chemmart Tramadol SR </PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>SR Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154396-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>154397</Austr>
				<PresentationName>Chemmart Tramadol SR </PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>SR Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154397-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>154400</Austr>
				<PresentationName>Chemmart Tramadol SR </PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/03/2011 10:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>SR Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154400-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158471</Austr>
				<PresentationName>Chemmart Tramadol</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Tramadol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/01/2012 16:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green and yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158471-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tramadol Hydrochloride (GA)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>141239</Austr>
				<PresentationName>GA Tramadol</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 12:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green and yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>141239-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>154407</Austr>
				<PresentationName>GA Tramadol SR</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 12:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154407-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>154408</Austr>
				<PresentationName>GA Tramadol SR</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 12:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154408-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>154409</Austr>
				<PresentationName>GA Tramadol SR</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/11/2013 12:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154409-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tramadol Hydrochloride (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>194539</Austr>
				<PresentationName>Tramadol SR generichealth</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2015 16:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>194539-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>194540</Austr>
				<PresentationName>Tramadol SR generichealth</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2015 16:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>194540-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>194541</Austr>
				<PresentationName>Tramadol SR generichealth</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/06/2015 16:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>194541-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tramadol Hydrochloride (GenRx)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>97458</Austr>
				<PresentationName>GenRx Tramadol</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tramadol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/07/2008 08:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>97458-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tramadol Hydrochloride (Mylan)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>133147</Austr>
				<PresentationName>Tramadol Mylan SR (formerly Tramedo SR)</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tramadol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/10/2008 08:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>almost white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TL 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133147-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>133157</Austr>
				<PresentationName>Tramadol Mylan SR (formerly Tramedo SR)			</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tramadol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/10/2008 08:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>almost white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>TL150</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133157-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>133158</Austr>
				<PresentationName>Tramadol Mylan SR (formerly Tramedo SR)			</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tramadol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/10/2008 07:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>almost white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>TL200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133158-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tramadol Hydrochloride (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>141240</Austr>
				<PresentationName>Tramadol Sandoz</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>26/04/2012 17:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green and yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>141240-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>99239</Austr>
				<PresentationName>Tramadol Sandoz SR</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tramadol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/10/2018 17:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green and white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>T R 100 R</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>99239-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>99252</Austr>
				<PresentationName>Tramadol Sandoz SR</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tramadol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/10/2018 17:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green and white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>T R 150 R</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>99252-A01-02-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>99252-B01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>99258</Austr>
				<PresentationName>Tramadol Sandoz SR</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tramadol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
						<VersionSequence>2</VersionSequence>
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						<DateEffective>22/10/2018 17:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green and white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>T R 200 R</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>99258-A01-02-BL600.jpg</ImageFileName>
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							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>99258-B01-02-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tramadol Hydrochloride (SCP)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>141238</Austr>
				<PresentationName>Tramadol SCP</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>29/11/2013 15:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green and yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>141238-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tramadol Hydrochloride (Terry White Chemists)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>154401</Austr>
				<PresentationName>Terry White Chemists Tramadol SR</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/03/2011 10:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>SR Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154401-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>154402</Austr>
				<PresentationName>Terry White Chemists Tramadol SR</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/03/2011 10:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>SR Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154402-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>154403</Austr>
				<PresentationName>Terry White Chemists Tramadol SR </PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/03/2011 10:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>SR Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154403-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158473</Austr>
				<PresentationName>Terry White Chemists Tramadol</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Tramadol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/01/2012 16:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green and yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158473-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tramadol Hydrochloride/Paracetamol (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>280699</Austr>
				<PresentationName>APO-Tramadol/Paracetamol</PresentationName>
    			<PresentionStrength>37.5mg/325mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Paracetamol,Tramadol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/04/2019 18:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>37.5-325</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>280699-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tramal</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>121845</Austr>
				<PresentationName>Tramal SR</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tramadol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/08/2008 11:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>T0</Side1Marking>
							<Side2Marking>GRUNENTHAL logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>121845-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>64011</Austr>
				<PresentationName>Tramal Capsules</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tramadol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/08/2008 15:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>green and yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>GRUNENTHAL logo</Side1Marking>
							<Side2Marking>GRUNENTHAL logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>64011-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>75947</Austr>
				<PresentationName>Tramal SR</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tramadol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/08/2008 11:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>T1</Side1Marking>
							<Side2Marking>GRUNENTHAL logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75947-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>75948</Austr>
				<PresentationName>Tramal SR</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tramadol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/08/2008 11:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>T2</Side1Marking>
							<Side2Marking>GRUNENTHAL logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75948-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>75949</Austr>
				<PresentationName>Tramal SR</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tramadol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/08/2008 11:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>deep orange to brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>T3</Side1Marking>
							<Side2Marking>GRUNENTHAL logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75949-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tramedo</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>114181</Austr>
				<PresentationName>Tramedo</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Tramadol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tramedo</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tramadol hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-03-25 15:25:12.0</ReleaseDate>
					</DocumentQualifiers>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>&#945;</Side1Marking>
							<Side2Marking>TL 50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>114181-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>114197</Austr>
				<PresentationName>Tramedo</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tramadol hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tramedo</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afctrame10322</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tramadol hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-03-25 15:25:12.0</ReleaseDate>
					</DocumentQualifiers>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>&#945;</Side1Marking>
							<Side2Marking>TL 50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>114197-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>154383</Austr>
				<PresentationName>Tramedo SR (New Formulation)</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tramedo SR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tramadol hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-09-29 14:03:24.0</ReleaseDate>
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				<Images>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>30/11/2022 16:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154383-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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				<Austr>154388</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<QualiferData></QualiferData>
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						<ActiveIngredient>tramadol hydrochloride</ActiveIngredient>
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						<VersionSequence>1</VersionSequence>
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						<DateEffective>30/11/2022 16:54</DateEffective>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
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			<Presentations>
				<Austr>154389</Austr>
				<PresentationName>Tramedo SR (New Formulation)</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
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			</Presentations>
		</Brand><Brand>
			<brandname>Tranalpha</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>198992</Austr>
				<PresentationName>Tranalpha</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Trandolapril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tranalpha</DocumentName>
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							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>trandolapril</ActiveIngredient>
						<ReleaseDate>2020-01-17 12:19:39.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light scarlet and rich yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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								<ImageFileName>198992-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>198993</Austr>
				<PresentationName>Tranalpha</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Trandolapril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tranalpha</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>trandolapril</ActiveIngredient>
						<ReleaseDate>2020-01-17 12:19:39.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light scarlet and light orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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								<ImageFileName>198993-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>198994</Austr>
				<PresentationName>Tranalpha</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Trandolapril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tranalpha</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>trandolapril</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
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							<Scoring></Scoring>
							<Shape></Shape>
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							<Views>
							<View>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>198995</Austr>
				<PresentationName>Tranalpha</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Trandolapril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Tranalpha</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>trandolapril</ActiveIngredient>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
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							<Scoring></Scoring>
							<Shape></Shape>
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							<Views>
							<View>
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			</Presentations>
		</Brand><Brand>
			<brandname>Trandolapril (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>135959</Austr>
				<PresentationName>Apo-Trandolapril</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Trandolapril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>15/06/2009 09:13</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange and ivory</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TR</Side1Marking>
							<Side2Marking>0.5</Side2Marking>
							<Views>
							<View>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>135968</Austr>
				<PresentationName>Apo-Trandolapril</PresentationName>
    			<PresentionStrength>1mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Trandolapril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange and light orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TR</Side1Marking>
							<Side2Marking>1</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>135978</Austr>
				<PresentationName>Apo-Trandolapril</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Trandolapril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<DateEffective>15/06/2009 09:15</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TR</Side1Marking>
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							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>135985</Austr>
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    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Trandolapril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
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						<DateEffective>15/06/2009 09:12</DateEffective>
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                    	<Phase>
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							<DoseForm>Capsules</DoseForm>
							<Colour>flesh</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TR</Side1Marking>
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							<Views>
							<View>
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		</Brand><Brand>
			<brandname>Trandolapril (GA)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>135957</Austr>
				<PresentationName>Trandolapril-GA</PresentationName>
    			<PresentionStrength>0.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
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                    	<Phase>
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							<DoseForm>Capsules</DoseForm>
							<Colour>orange and ivory</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TR</Side1Marking>
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							<Views>
							<View>
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			<Presentations>
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				<PresentationName>Trandolapril-GA</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange and light orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TR</Side1Marking>
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							<Views>
							<View>
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			<Presentations>
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				<PresentationName>Trandolapril-GA</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
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							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>TR</Side1Marking>
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							<Views>
							<View>
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			<Presentations>
				<Austr>135983</Austr>
				<PresentationName>Trandolapril-GA</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Side1Marking>TR</Side1Marking>
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							<Views>
							<View>
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		</Brand><Brand>
			<brandname>Tranexamic Acid (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
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				<Austr>272732</Austr>
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    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>04/07/2017 15:16</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to slightly yellowish</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>TXA 500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>272732-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trental</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>81197</Austr>
				<PresentationName>Trental 400</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oxpentifylline</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Trental 400</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swctrent10420</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>pentoxifylline (oxpentifylline)</ActiveIngredient>
						<ReleaseDate>2020-04-30 14:50:33.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/06/2008 15:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>ATA</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>81197-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Triasyn</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>67183</Austr>
				<PresentationName>Triasyn</PresentationName>
    			<PresentionStrength>5mg/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril,Felodipine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Triasyn</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swctrias11219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>felodipine with ramipril</ActiveIngredient>
						<ReleaseDate>2019-12-20 11:37:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish-brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>H OE</Side1Marking>
							<Side2Marking>5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>67183-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>67184</Austr>
				<PresentationName>Triasyn</PresentationName>
    			<PresentionStrength>2.5mg/2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril,Felodipine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Triasyn</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swctrias11219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>felodipine with ramipril</ActiveIngredient>
						<ReleaseDate>2019-12-20 11:37:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>apricot</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>H OD</Side1Marking>
							<Side2Marking>2.5</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>67184-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trifeme</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>40133</Austr>
				<PresentationName>Trifeme</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ethinyloestradiol,Levonorgestrel</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Trifeme</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfctrift11219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levonorgestrel with ethinylestradiol</ActiveIngredient>
						<ReleaseDate>2019-12-13 09:22:51.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/10/2011 16:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>40133-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>40133-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>3</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>40133-C03-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>4</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>40133-C04-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trileptal</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>76200</Austr>
				<PresentationName>Trileptal</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oxcarbazepine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Trileptal</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvctrior10620</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>oxcarbazepine</ActiveIngredient>
						<ReleaseDate>2020-07-05 21:45:32.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>10/12/2008 12:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale green</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>T D</Side1Marking>
							<Side2Marking>C G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>76200-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>76201</Austr>
				<PresentationName>Trileptal</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oxcarbazepine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Trileptal</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvctrior10620</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>oxcarbazepine</ActiveIngredient>
						<ReleaseDate>2020-07-05 21:45:32.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>10/12/2008 12:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>TE TE</Side1Marking>
							<Side2Marking>CG CG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>76201-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>76202</Austr>
				<PresentationName>Trileptal</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oxcarbazepine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Trileptal</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvctrior10620</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>oxcarbazepine</ActiveIngredient>
						<ReleaseDate>2020-07-05 21:45:32.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/01/2009 10:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>TF TF</Side1Marking>
							<Side2Marking>CG CG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>76202-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trimethoprim (Mylan)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>338350</Austr>
				<PresentationName>Trimethoprim Mylan</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>trimethoprim</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Trimethoprim Mylan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afctripm10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>trimethoprim</ActiveIngredient>
						<ReleaseDate>2022-05-11 16:06:35.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/03/2022 12:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TM 300</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>338350-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Triphasil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10419</Austr>
				<PresentationName>Triphasil</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ethinyloestradiol,Levonorgestrel</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Triphasil</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfctript11219</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>levonorgestrel with ethinylestradiol</ActiveIngredient>
						<ReleaseDate>2019-12-13 10:47:09.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/10/2011 16:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10419-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10419-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>3</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10419-C03-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>4</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10419-C04-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Triprim</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>11009</Austr>
				<PresentationName>Triprim Tablets</PresentationName>
    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 09:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>TRIPRIM</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>11009-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Triquilar</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10722</Austr>
				<PresentationName>Triquilar ED</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>26/11/2014 12:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10722-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10722-C02-02-BL600.jpg</ImageFileName>
							</View>
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							<PhaseItem>3</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>ochre</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10722-C03-02-BL600.jpg</ImageFileName>
							</View>
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							<PhaseItem>4</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10722-C04-02-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Trisequens</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>192476</Austr>
				<PresentationName>Trisequens</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>dial dispenser pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<VersionSequence>1</VersionSequence>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NOVO 280</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192476-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NOVO 281</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192476-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>3</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NOVO 282</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>192476-C03-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>45155</Austr>
				<PresentationName>Trisequens</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>dial dispenser pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/10/2008 09:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NOVO 280</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>45155-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NOVO 281</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>45155-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>3</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NOVO 282</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>45155-C03-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tritace</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>34515</Austr>
				<PresentationName>Tritace</PresentationName>
    			<PresentionStrength>1.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tritace</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
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								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>ramipril</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/01/2009 16:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to pale yellowish white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>1.25 HMN</Side1Marking>
							<Side2Marking>1.25 logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>34515-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>56537</Austr>
				<PresentationName>Tritace</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tritace</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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						</DocumentTypes>
						<ActiveIngredient>ramipril</ActiveIngredient>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>08/07/2008 13:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>2.5 HMR</Side1Marking>
							<Side2Marking>2.5 logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>56537-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>56538</Austr>
				<PresentationName>Tritace</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tritace</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ramipril</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/02/2009 09:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>5 HMP</Side1Marking>
							<Side2Marking>5 logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>56538-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>75202</Austr>
				<PresentationName>Tritace</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tritace</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ramipril</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75202-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>79253</Austr>
				<PresentationName>Tritace</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tritace</DocumentName>
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							<AvailableFormats>
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						</DocumentTypes>
						<ActiveIngredient>ramipril</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/01/2009 16:27</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to pale yellowish white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>HMO HMO</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>79253-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Triumeq</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>218644</Austr>
				<PresentationName>Triumeq</PresentationName>
    			<PresentionStrength>50mg/600mg/300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Lamivudine,Abacavir sulfate,Dolutegravir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Triumeq</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
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						<ActiveIngredient>dolutegravir with abacavir and lamivudine</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/09/2016 10:43</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>purple</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>572 Tri</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>218644-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
		</Brand><Brand>
			<brandname>Trizivir</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>78348</Austr>
				<PresentationName>Trizivir</PresentationName>
    			<PresentionStrength>300/150/300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Zidovudine,Lamivudine,Abacavir sulfate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 15:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue/green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>GX LL1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>78348-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
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			</Presentations>
		</Brand><Brand>
			<brandname>Trovas</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>179821</Austr>
				<PresentationName>Trovas</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/10/2012 17:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>AS80</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179821-C01-01-BL600.jpg</ImageFileName>
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			</Presentations>
			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/04/2012 16:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>AS20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179829-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179834</Austr>
				<PresentationName>Trovas</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/10/2012 17:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>AS20</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179834-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179840</Austr>
				<PresentationName>Trovas</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/04/2012 16:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>AS40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179840-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179844</Austr>
				<PresentationName>Trovas</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/10/2012 16:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>AS10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179844-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179846</Austr>
				<PresentationName>Trovas</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/04/2012 16:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>AS10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179846-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179847</Austr>
				<PresentationName>Trovas</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/04/2012 16:13</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>AS80</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179847-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179860</Austr>
				<PresentationName>Trovas</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Atorvastatin calcium trihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/10/2012 17:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking>AS40</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179860-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Analgesic Calmative</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>217762</Austr>
				<PresentationName>Trust Analgesic Calmative</PresentationName>
    			<PresentionStrength>500mg/10mg/5.1mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2015 11:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>217762-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Aspirin EC</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>177615</Austr>
				<PresentationName>Trust Aspirin EC</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2015 12:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking>heart shape</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>177615-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Cetirizine</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>160460</Austr>
				<PresentationName>Trust Cetirizine</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2015 12:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>M+</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>160460-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Cold Relief</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>219373</Austr>
				<PresentationName>Trust Cold Relief</PresentationName>
    			<PresentionStrength>500mg/2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2015 12:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>219373-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust ColoxEase</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>250052</Austr>
				<PresentationName>Trust ColoxEase</PresentationName>
    			<PresentionStrength>50mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/10/2016 09:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>250052-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Day/Night Cold Relief</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>151639</Austr>
				<PresentationName>Trust Day/Night Cold Relief</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2015 12:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>151639-B01-01-BL600.jpg</ImageFileName>
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							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>151639-A02-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>151639-B02-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust DeWorm</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>175665</Austr>
				<PresentationName>Trust DeWorm</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Difenac</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>247652</Austr>
				<PresentationName>Trust Difenac</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/01/2016 10:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
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			</Presentations>
		</Brand><Brand>
			<brandname>Trust Fenmol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>264192</Austr>
				<PresentationName>Trust Fenmol</PresentationName>
    			<PresentionStrength>200mg/500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>264192-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Fexit</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>208325</Austr>
				<PresentationName>Trust Fexit</PresentationName>
    			<PresentionStrength>120mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2015 12:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>caplet-shaped</Shape>
							<Side1Marking>120</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>208325-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>208326</Austr>
				<PresentationName>Trust Fexit</PresentationName>
    			<PresentionStrength>180mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2015 12:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>caplet-shaped</Shape>
							<Side1Marking>180</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>208326-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Glucosamine</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>158128</Austr>
				<PresentationName>Trust Glucosamine</PresentationName>
    			<PresentionStrength>1500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2015 12:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158128-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Ibuprofen</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>206743</Austr>
				<PresentationName>Trust Ibuprofen</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2015 12:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>206743-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Ibuprofen Double Strength</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>205746</Austr>
				<PresentationName>Trust Ibuprofen Double Strength</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2015 12:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>pillow-shaped</Shape>
							<Side1Marking>236</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>205746-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Ibuprofen Plus Codeine</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>175264</Austr>
				<PresentationName>Trust Ibuprofen Plus Codeine</PresentationName>
    			<PresentionStrength>200mg/12.8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2015 12:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>175264-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Koloxeze</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>176294</Austr>
				<PresentationName>Trust Koloxeze</PresentationName>
    			<PresentionStrength>50mg/8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2015 12:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>176294-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Loratadine</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>161830</Austr>
				<PresentationName>Trust Loratadine</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2015 12:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>161830-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Migraine Headache &amp; Nausea Relief</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>186862</Austr>
				<PresentationName>Trust Migraine Headache &amp; Nausea Relief</PresentationName>
    			<PresentionStrength>500mg/5.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2015 12:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>186862-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>186862-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Naproxen</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>207745</Austr>
				<PresentationName>Trust Naproxen</PresentationName>
    			<PresentionStrength>275mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2015 12:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>207745-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Osteo D</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>228118</Austr>
				<PresentationName>Trust Osteo D</PresentationName>
    			<PresentionStrength>1000IU</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2015 12:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>transparent yellow</Colour>
							<Scoring></Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>228118-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Restamine</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>207746</Austr>
				<PresentationName>Trust Restamine</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2015 12:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>207746-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Sinus &amp; Nasal Decongestant</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>233000</Austr>
				<PresentationName>Trust Sinus &amp; Nasal Decongestant</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2015 12:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>233000-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Stomach Ease Forte</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>222897</Austr>
				<PresentationName>Trust Stomach Ease Forte</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2015 12:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>off white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>222897-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Stomache Ease</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>232966</Austr>
				<PresentationName>Trust Stomache Ease</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/10/2016 09:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>232966-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Strong Pain Relief</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>201679</Austr>
				<PresentationName>Trust Strong Pain Relief</PresentationName>
    			<PresentionStrength>500mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/03/2016 12:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>201679-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Thrombix</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>175831</Austr>
				<PresentationName>Trust Thrombix</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/08/2012 12:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>heart-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>175831-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Trust Umol Extra</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>218719</Austr>
				<PresentationName>Trust Umol Extra</PresentationName>
    			<PresentionStrength>500mg/65mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/10/2015 12:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>caplet-shaped</Shape>
							<Side1Marking>65</Side1Marking>
							<Side2Marking>500</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>218719-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tryzan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>127085</Austr>
				<PresentationName>Tryzan</PresentationName>
    			<PresentionStrength>1.25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tryzan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ramipril</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>RM 1.25</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127085-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127088</Austr>
				<PresentationName>Tryzan</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tryzan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ramipril</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/07/2012 16:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>RM 2.5</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127088-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127152</Austr>
				<PresentationName>Tryzan</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tryzan</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ramipril</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
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						<DateEffective>20/07/2012 16:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and swedish orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>RM 5</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127152-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>127153</Austr>
				<PresentationName>Tryzan</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tryzan</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ramipril</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
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						<DateEffective>20/07/2012 16:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>RM 10</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>127153-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>129873</Austr>
				<PresentationName>Tryzan</PresentationName>
    			<PresentionStrength>1.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tryzan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ramipril</ActiveIngredient>
						<ReleaseDate>2022-07-06 15:39:40.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/08/2008 10:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>129873-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>129916</Austr>
				<PresentationName>Tryzan</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tryzan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afctryca10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ramipril</ActiveIngredient>
						<ReleaseDate>2022-07-06 15:39:40.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/08/2008 10:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>R 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>129916-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>129918</Austr>
				<PresentationName>Tryzan</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tryzan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afctryca10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ramipril</ActiveIngredient>
						<ReleaseDate>2022-07-06 15:39:40.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/08/2008 10:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>R 3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>129918-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>129921</Austr>
				<PresentationName>Tryzan</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ramipril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Tryzan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afctryca10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ramipril</ActiveIngredient>
						<ReleaseDate>2022-07-06 15:39:40.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/08/2008 10:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>R 4</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>129921-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Twynsta</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>166263</Austr>
				<PresentationName>Twynsta</PresentationName>
    			<PresentionStrength>80mg/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>amlodipine besilate,telmisartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Twynsta</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>telmisartan with amlodipine besilate</ActiveIngredient>
						<ReleaseDate>2022-07-20 17:52:38.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/01/2012 10:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white and blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>company logo A3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166263-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166264</Austr>
				<PresentationName>Twynsta</PresentationName>
    			<PresentionStrength>40mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>telmisartan,amlodipine besilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Twynsta</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>telmisartan with amlodipine besilate</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>19/01/2012 10:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
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							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>company logo A2</Side1Marking>
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			<Presentations>
				<Austr>166265</Austr>
				<PresentationName>Twynsta</PresentationName>
    			<PresentionStrength>40mg/5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient>telmisartan,amlodipine besilate</TGAIngredient>
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						<VersionSequence>1</VersionSequence>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white and blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>company logo A1</Side1Marking>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>166266</Austr>
				<PresentationName>Twynsta</PresentationName>
    			<PresentionStrength>80mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>telmisartan,amlodipine besilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
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						<ActiveIngredient>telmisartan with amlodipine besilate</ActiveIngredient>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white and blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>company logo A4</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Tykerb</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>132305</Austr>
				<PresentationName>Tykerb</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lapatinib ditosylate monohydrate</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>14/08/2008 15:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>GSXJG</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>132305-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>185997</Austr>
				<PresentationName>Tykerb</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Lapatinib ditosylate monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<QualiferData></QualiferData>
						<DocumentName>Tykerb</DocumentName>
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							<AvailableFormats>
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						<ActiveIngredient>lapatinib ditosilate monohydrate</ActiveIngredient>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>02/05/2016 17:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>GS XJG</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ulcaid</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>116927</Austr>
				<PresentationName>Ulcaid</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/02/2009 10:12</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>creamish-yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>RAN 150</Side1Marking>
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							<Views>
							<View>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ultibro Breezhaler 110/50</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>206449</Austr>
				<PresentationName>Ultibro Breezhaler 110/50</PresentationName>
    			<PresentionStrength>110mcg/50mcg</PresentionStrength>
    			<PresentationForm>Inhalation Capsule</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Indacaterol maleate,Glycopyrronium bromide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Ultibro Breezhaler 110/50</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
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							<Shape></Shape>
							<Side1Marking>company logo</Side1Marking>
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			</Presentations>
		</Brand><Brand>
			<brandname>Uremide</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>17704</Austr>
				<PresentationName>Uremide</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Frusemide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>furosemide (frusemide)</ActiveIngredient>
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							<DoseForm>Tablets</DoseForm>
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							<Side1Marking>FE 40</Side1Marking>
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							<Views>
							<View>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Urex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>13475</Austr>
				<PresentationName>Urex M</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>196972</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
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							<Views>
							<View>
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							<View>
								<ViewLabel>B</ViewLabel>
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							</Views>
						</Phase>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>34494</Austr>
				<PresentationName>Urex</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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							<View>
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						</Phase>
					</Versions>
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			</Presentations>
			<Presentations>
				<Austr>56090</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
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							<View>
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							<View>
								<ViewLabel>B</ViewLabel>
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		</Brand><Brand>
			<brandname>Urocarb</brandname>
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			<Presentations>
				<Austr>14861</Austr>
				<PresentationName>Urocarb</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient></TGAIngredient>
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		</Brand><Brand>
			<brandname>Urocit</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>75406</Austr>
				<PresentationName>Urocit K</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<View>
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		</Brand><Brand>
			<brandname>Urorec</brandname>
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			<Presentations>
				<Austr>275265</Austr>
				<PresentationName>Urorec</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Urorec</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>yncurore21021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>silodosin</ActiveIngredient>
						<ReleaseDate>2021-10-06 16:20:09.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/11/2017 09:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>275265-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ursodeoxycholic acid (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>276339</Austr>
				<PresentationName>APO-Ursodeoxycholic Acid</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ursodeoxycholic acid</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>16/11/2017 11:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>276339-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ursodeoxycholic acid (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>232480</Austr>
				<PresentationName>Ursodox GH</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/05/2017 15:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>232480-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ursofalk</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>66042</Austr>
				<PresentationName>Ursofalk</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/06/2009 15:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>66042-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Vaclovir</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>153822</Austr>
				<PresentationName>Vaclovir</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valaciclovir hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType>Pack Size</QualifierType>
						<QualiferData>10,30</QualiferData>
						<DocumentName>Vaclovir (Herpes Simplex)</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcvachs10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>valaciclovir hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-08-10 13:46:26.0</ReleaseDate>
					</DocumentQualifiers>
					<DocumentQualifiers>
						<QualifierType>Pack Size</QualifierType>
						<QualiferData>42</QualiferData>
						<DocumentName>Vaclovir (Cytomegalovirus)</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcvaclc10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>valaciclovir hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-08-10 13:46:06.0</ReleaseDate>
					</DocumentQualifiers>
					<DocumentQualifiers>
						<QualifierType>Pack Size</QualifierType>
						<QualiferData>42</QualiferData>
						<DocumentName>Vaclovir (Herpes Zoster / Herpes Labialis)</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcvachz10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>valaciclovir hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-08-10 13:46:43.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/07/2011 13:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153822-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>153823</Austr>
				<PresentationName>Vaclovir</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Valaciclovir hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType>Pack Size</QualifierType>
						<QualiferData>30</QualiferData>
						<DocumentName>Vaclovir (Herpes Simplex)</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcvachs10822</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>valaciclovir hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-08-10 13:46:26.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>27/12/2012 16:08</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153823-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Vagifem</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>10265</Austr>
				<PresentationName>Vagifem</PresentationName>
    			<PresentionStrength>25 mcg</PresentionStrength>
    			<PresentationForm>Pessary</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/10/2008 09:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Pessary</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>NOVO 279</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>10265-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Valaciclovir hydrochloride (Actavis)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>170177</Austr>
				<PresentationName>Valaciclovir Actavis</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/12/2014 14:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>VC 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>170177-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Valaciclovir hydrochloride (Amneal)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>173287</Austr>
				<PresentationName>Valaciclovir Pfizer</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valaciclovir hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>28/06/2012 12:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>F</Side1Marking>
							<Side2Marking>93</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>173287-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Valaciclovir hydrochloride (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>158906</Austr>
				<PresentationName>APO-Valaciclovir</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valaciclovir hydrochloride monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>17/06/2011 11:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>VAL 1000</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158906-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158911</Austr>
				<PresentationName>APO-Valaciclovir</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valaciclovir hydrochloride monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/06/2011 13:25</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>VAL 500</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158911-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>177375</Austr>
				<PresentationName>Valaciclovir Apotex</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>valaciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/04/2020 09:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>V 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>177375-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Valaciclovir hydrochloride (Chemmart)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>158913</Austr>
				<PresentationName>Chemmart Valaciclovir</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Valaciclovir hydrochloride monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>17/06/2011 10:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>VAL 500</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158913-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Valaciclovir hydrochloride (Generic Health)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>170178</Austr>
				<PresentationName>Valaciclovir generichealth</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>VC 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>170178-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Valaciclovir hydrochloride (Ranbaxy)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>142803</Austr>
				<PresentationName>Valaciclovir RBX</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>12/09/2011 09:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>V 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>142803-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Valaciclovir hydrochloride (Sandoz)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>154460</Austr>
				<PresentationName>Valaciclovir SZ</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Valaciclovir hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/06/2011 14:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154460-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>154464</Austr>
				<PresentationName>Valaciclovir Sandoz</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Valaciclovir hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>06/06/2011 14:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>154464-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Valacor</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>177373</Austr>
				<PresentationName>Valacor</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>27/07/2011 13:20</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>V 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>177373-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Valcyte</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>82903</Austr>
				<PresentationName>Valcyte</PresentationName>
    			<PresentionStrength>450mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Valganciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Valcyte Tablets</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>rocvalcy11020</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>valganciclovir hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-10-15 12:06:42.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/09/2008 10:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>VGC</Side1Marking>
							<Side2Marking>450</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>82903-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Valdoxan</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>159712</Austr>
				<PresentationName>Valdoxan</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Agomelatine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Valdoxan</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>secvaldx30522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>agomelatine</ActiveIngredient>
						<ReleaseDate>2022-05-31 20:42:41.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>28/10/2011 14:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange-yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>Company Logo</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>159712-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Valette</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>122788</Austr>
				<PresentationName>Valette</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2010 10:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>122788-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>122788-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Valganciclovir (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>227605</Austr>
				<PresentationName>Valganciclovir Sandoz</PresentationName>
    			<PresentionStrength>450mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valganciclovir</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/10/2017 14:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>J</Side1Marking>
							<Side2Marking>156</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>227605-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Valganciclovir (Viatris)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>218477</Austr>
				<PresentationName>Valganciclovir Viatris</PresentationName>
    			<PresentionStrength>450mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Valganciclovir hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Valganciclovir Viatris</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcvalgm10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>valganciclovir hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-05-11 16:06:46.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/12/2018 10:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>V45</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>218477-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Valium</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>48566</Austr>
				<PresentationName>Valium</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Diazepam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Valium</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>iycvaliu10522</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>diazepam</ActiveIngredient>
						<ReleaseDate>2022-06-14 15:30:54.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>01/09/2008 16:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROCHE 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>48566-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>66129</Austr>
				<PresentationName>Valium</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Diazepam</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 14:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ROCHE 2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>66129-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Valpam</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>80812</Austr>
				<PresentationName>Valpam</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/10/2018 14:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DZ 5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>80812-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Valpam</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>80809</Austr>
				<PresentationName>Valpam</PresentationName>
    			<PresentionStrength>2mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 10:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DZ 2</Side1Marking>
							<Side2Marking>Arrow symbol</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>80809-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>80811</Austr>
				<PresentationName>Valpam</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 10:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DZ 5</Side1Marking>
							<Side2Marking>Arrow symbol</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>80811-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Valprease</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>153053</Austr>
				<PresentationName>Valprease</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/10/2018 14:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>purple</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>153053-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>153054</Austr>
				<PresentationName>Valprease</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/10/2018 14:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>purple</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>A</ViewLabel>
								<ImageFileName>153054-A01-01-BL600.jpg</ImageFileName>
							</View>
							<View>
								<ViewLabel>B</ViewLabel>
    							<ImageFileName>153054-B01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Valsartan (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>185806</Austr>
				<PresentationName>APO-Valsartan</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 10:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>modified capsule-shaped</Shape>
							<Side1Marking>VA 40</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>185806-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>185814</Austr>
				<PresentationName>APO-Valsartan</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 10:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>VA 80</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>185814-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>185821</Austr>
				<PresentationName>APO-Valsartan</PresentationName>
    			<PresentionStrength>160mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 10:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified capsule-shaped</Shape>
							<Side1Marking>VA 160</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>185821-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>185826</Austr>
				<PresentationName>APO-Valsartan</PresentationName>
    			<PresentionStrength>320mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/01/2015 10:38</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark grey violet</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>VA 320</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>185826-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Valsartan/HCTZ (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>202344</Austr>
				<PresentationName>APO-Valsartan HCTZ</PresentationName>
    			<PresentionStrength>320/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>320/12.5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>202344-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>202345</Austr>
				<PresentationName>APO-Valsartan HCTZ</PresentationName>
    			<PresentionStrength>320/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>320/25</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>202345-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>202354</Austr>
				<PresentationName>APO-Valsartan HCTZ</PresentationName>
    			<PresentionStrength>160/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valsartan,Hydrochlorothiazide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:52</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified capsule shaped</Shape>
							<Side1Marking>160/12.5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>202354-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>222295</Austr>
				<PresentationName>APO-Valsartan HCTZ</PresentationName>
    			<PresentionStrength>160mg/25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/05/2017 13:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified capsule shaped</Shape>
							<Side1Marking>160/25</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>222295-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>222296</Austr>
				<PresentationName>APO-Valsartan HCTZ</PresentationName>
    			<PresentionStrength>80mg/12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Hydrochlorothiazide,Valsartan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/05/2017 13:57</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified capsule shaped</Shape>
							<Side1Marking>80/12.5</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>222296-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Valtrex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>73917</Austr>
				<PresentationName>Valtrex</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Valaciclovir hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>15/06/2012 16:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elongated</Shape>
							<Side1Marking>GX CF1</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73917-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>73920</Austr>
				<PresentationName>Valtrex</PresentationName>
    			<PresentionStrength>1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Valaciclovir hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>31/10/2008 11:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>elongated</Shape>
							<Side1Marking>GX CF2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73920-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Vasafil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>172068</Austr>
				<PresentationName>Vasafil</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/10/2018 14:05</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SD 100</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>172068-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>172073</Austr>
				<PresentationName>Vasafil</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/10/2018 14:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>green</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SD 25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>172073-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Vasocardol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>68922</Austr>
				<PresentationName>Vasocardol CD</PresentationName>
    			<PresentionStrength>180mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Diltiazem hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Vasocardol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcvasoc10621</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>diltiazem hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-06-25 09:06:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>dark blue and light aqua blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>68922-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>68925</Austr>
				<PresentationName>Vasocardol CD</PresentationName>
    			<PresentionStrength>240mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Diltiazem hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Vasocardol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcvasoc10621</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>diltiazem hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-06-25 09:06:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>dark blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>68925-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>73180</Austr>
				<PresentationName>Vasocardol</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Diltiazem hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Vasocardol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcvasoc10621</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>diltiazem hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-06-25 09:06:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light yellow, speckled</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>17 72</Side1Marking>
							<Side2Marking>MARION</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>73180-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>75253</Austr>
				<PresentationName>Vasocardol CD</PresentationName>
    			<PresentionStrength>360mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Diltiazem hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Vasocardol</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcvasoc10621</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>diltiazem hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-06-25 09:06:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white and light blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>75253-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Vedafil</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>162805</Austr>
				<PresentationName>Vedafil</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sildenafil citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Vedafil</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcvedaf10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>sildenafil citrate</ActiveIngredient>
						<ReleaseDate>2022-07-18 09:29:24.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/11/2016 16:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SL 50</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>162805-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>162806</Austr>
				<PresentationName>Vedafil</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sildenafil citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Vedafil</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcvedaf10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>sildenafil citrate</ActiveIngredient>
						<ReleaseDate>2022-07-18 09:29:24.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/12/2018 16:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SL 100</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>162806-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>162807</Austr>
				<PresentationName>Vedafil</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sildenafil citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Vedafil</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afcvedaf10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>sildenafil citrate</ActiveIngredient>
						<ReleaseDate>2022-07-18 09:29:24.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/11/2016 16:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>SL 25</Side1Marking>
							<Side2Marking>M</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>162807-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Vedilol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>136623</Austr>
				<PresentationName>Vedilol</PresentationName>
    			<PresentionStrength>3.125mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2011 14:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CL 3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>136623-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>136873</Austr>
				<PresentationName>Vedilol</PresentationName>
    			<PresentionStrength>6.25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2011 14:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CL 6</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>136873-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>137280</Austr>
				<PresentationName>Vedilol</PresentationName>
    			<PresentionStrength>12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2011 14:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CL 12</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>137280-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>137281</Austr>
				<PresentationName>Vedilol</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/03/2011 14:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>CL 25</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>137281-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Velmetia</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>220155</Austr>
				<PresentationName>Velmetia</PresentationName>
    			<PresentionStrength>50mg/500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride,sitagliptin phosphate monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Velmetia</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>sitagliptin phosphate monohydrate with metformin hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-07-08 15:10:47.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>02/12/2022 08:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>575</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>220155-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>220156</Austr>
				<PresentationName>Velmetia</PresentationName>
    			<PresentionStrength>50mg/850mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>sitagliptin phosphate monohydrate,Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Velmetia</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>sitagliptin phosphate monohydrate with metformin hydrochloride</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>02/12/2022 08:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>515</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>220156-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>220157</Austr>
				<PresentationName>Velmetia</PresentationName>
    			<PresentionStrength>50mg/1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride,sitagliptin phosphate monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Velmetia</DocumentName>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>sitagliptin phosphate monohydrate with metformin hydrochloride</ActiveIngredient>
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					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
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						<VersionStatus>Current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>577</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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		</Brand><Brand>
			<brandname>Venlafaxine (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>151875</Austr>
				<PresentationName>Venlafaxine Sandoz XR</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>scarlet opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151875-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>151880</Austr>
				<PresentationName>Venlafaxine Sandoz XR</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<VersionStatus>Current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>flesh opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151880-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Venlafaxine SR (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>160293</Austr>
				<PresentationName>Venlafaxine AN SR</PresentationName>
    			<PresentionStrength>37.5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>26/07/2017 16:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>grey/peach</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>radial circular bands</Side1Marking>
							<Side2Marking>radial circular bands</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>160293-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>160294</Austr>
				<PresentationName>Venlafaxine AN SR</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>peach</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>radial circular bands</Side1Marking>
							<Side2Marking>radial circular bands</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>160294-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>160295</Austr>
				<PresentationName>Venlafaxine AN SR</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>26/07/2017 16:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>dark orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>radial circular bands</Side1Marking>
							<Side2Marking>radial circular bands</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>160295-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Venlafaxine SR (SCP)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>160297</Austr>
				<PresentationName>Venlafaxine SR SCP</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>peach</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>radial circular bands</Side1Marking>
							<Side2Marking>radial circular bands</Side2Marking>
							<Views>
							<View>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>160298</Austr>
				<PresentationName>Venlafaxine SR SCP</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>dark orange</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>radial circular bands</Side1Marking>
							<Side2Marking>radial circular bands</Side2Marking>
							<Views>
							<View>
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								<ImageFileName>160298-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Venlafaxine XR (Actavis)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>200745</Austr>
				<PresentationName>Venlafaxine Actavis XR</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
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							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>radial circular bands</Side1Marking>
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							<Views>
							<View>
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			</Presentations>
			<Presentations>
				<Austr>200746</Austr>
				<PresentationName>Venlafaxine Actavis XR</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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					<Versions>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>peach</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>radial circular bands</Side1Marking>
							<Side2Marking>radial circular bands</Side2Marking>
							<Views>
							<View>
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				</Images>
			</Presentations>
			<Presentations>
				<Austr>200747</Austr>
				<PresentationName>Venlafaxine Actavis XR</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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                    	<Phase>
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							<DoseForm>Capsules</DoseForm>
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							<Shape></Shape>
							<Side1Marking>radial circular bands</Side1Marking>
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							<Views>
							<View>
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				</Images>
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		</Brand><Brand>
			<brandname>Venlafaxine XR (Apotex)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>286957</Austr>
				<PresentationName>APO-Venlafaxine XR</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Venlafaxine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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							<DoseForm>Capsules</DoseForm>
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							<Shape></Shape>
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			<Presentations>
				<Austr>286958</Austr>
				<PresentationName>APO-Venlafaxine XR </PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Venlafaxine hydrochloride</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<brandname>Venlafaxine XR (Blooms the Chemist)</brandname>
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			<Presentations>
				<Austr>286955</Austr>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
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			<brandname>Venlafaxine XR (Chemmart)</brandname>
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			<Presentations>
				<Austr>177458</Austr>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>18/06/2012 14:58</DateEffective>
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							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Venlafaxine XR (Generic Health)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>151876</Austr>
				<PresentationName>Venlafaxine XR generichealth</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>01/10/2012 12:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>scarlet opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151876-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>151884</Austr>
				<PresentationName>Venlafaxine XR generichealth</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>01/10/2012 12:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>flesh opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151884-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Venlafaxine XR (Terry White Chemists)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>177460</Austr>
				<PresentationName>Terry White Chemists Venlafaxine XR</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Venlafaxine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>18/06/2012 14:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque flesh-coloured</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>177460-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>177461</Austr>
				<PresentationName>Terry White Chemists Venlafaxine XR</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Venlafaxine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>18/06/2012 14:59</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque scarlet-coloured</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>177461-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Venlexor XR</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>151874</Austr>
				<PresentationName>Venlexor XR</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/06/2012 08:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsule</DoseForm>
							<Colour>scarlet opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151874-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>151885</Austr>
				<PresentationName>Venlexor XR</PresentationName>
    			<PresentionStrength>75mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/06/2012 08:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsule</DoseForm>
							<Colour>flesh opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151885-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ventolin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>12530</Austr>
				<PresentationName>Ventolin Rotacaps</PresentationName>
    			<PresentionStrength>200mcg</PresentionStrength>
    			<PresentationForm>Rotacaps</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>strip pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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						<DocumentName>Ventolin Rotacaps</DocumentName>
						<DocumentTypes>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>salbutamol sulfate</ActiveIngredient>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>pale blue and transparent</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>VENTOLIN 200</Side1Marking>
							<Side2Marking>VENTOLIN 200</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
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			</Presentations>
		</Brand><Brand>
			<brandname>Veracaps</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>41033</Austr>
				<PresentationName>Veracap SR</PresentationName>
    			<PresentionStrength>160mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-10 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>red/transparent</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>160</Side1Marking>
							<Side2Marking>SR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>41033-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>41035</Austr>
				<PresentationName>Veracap SR</PresentationName>
    			<PresentionStrength>240mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-11-10 00:00:00'}</WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque brown/yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>240</Side1Marking>
							<Side2Marking>SR</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>41035-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Verapamil (Mylan)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>80443</Austr>
				<PresentationName>Verapamil Mylan</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-03-21 00:00:00'}</WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Verapamil hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
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						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>VL 40</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>80443-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>80444</Austr>
				<PresentationName>Verapamil Mylan</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate>{ts '2022-03-21 00:00:00'}</WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Verapamil hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>orange-yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>VL 80</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>80444-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
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			</Presentations>
		</Brand><Brand>
			<brandname>Vermox</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>125654</Austr>
				<PresentationName>Vermox</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/06/2012 15:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>slightly orange</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>125654-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>176298</Austr>
				<PresentationName>Vermox Choc Chews</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>21/06/2012 15:56</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>lightly speckled chocolate brown</Colour>
							<Scoring>scored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>176298-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Vesanoid</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>53160</Austr>
				<PresentationName>Vesanoid</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Tretinoin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 15:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>orange-yellow and reddish-brown</Colour>
							<Scoring></Scoring>
							<Shape>oval</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>53160-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
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			</Presentations>
		</Brand><Brand>
			<brandname>Vesicare</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>117217</Austr>
				<PresentationName>Vesicare</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Solifenacin succinate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<brandname>Viagra</brandname>
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			<Presentations>
				<Austr>64434</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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   				<WithdrawalDate></WithdrawalDate>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>salmon</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SP</Side1Marking>
							<Side2Marking>150</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151814-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>151818</Austr>
				<PresentationName>Vimpat</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/08/2010 11:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pinkish</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SP</Side1Marking>
							<Side2Marking>50</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>151818-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Viramune</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>176980</Austr>
				<PresentationName>Viramune XR</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>nevirapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Viramune XR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>bycvirax11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>nevirapine</ActiveIngredient>
						<ReleaseDate>2021-11-03 12:22:08.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>12/04/2012 14:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>V04</Side1Marking>
							<Side2Marking>BI tower logo</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>176980-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Vivotif</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>118758</Austr>
				<PresentationName>Vivotif</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Salmonella typhi</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>25/08/2008 11:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>salmon pink and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>118758-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>158130</Austr>
				<PresentationName>Vivotif</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Salmonella typhi</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/07/2010 09:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsule</DoseForm>
							<Colour>salmon pink and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>158130-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Volibris</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>143739</Austr>
				<PresentationName>Volibris</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ambrisentan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Volibris</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gwcvolbr10221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ambrisentan</ActiveIngredient>
						<ReleaseDate>2021-02-17 10:47:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>17/12/2010 13:58</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>deep pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>KE3</Side1Marking>
							<Side2Marking>GS</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>143739-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>143743</Austr>
				<PresentationName>Volibris</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ambrisentan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Volibris</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gwcvolbr10221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ambrisentan</ActiveIngredient>
						<ReleaseDate>2021-02-17 10:47:37.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>17/12/2010 13:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>square</Shape>
							<Side1Marking>K2C</Side1Marking>
							<Side2Marking>GS</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>143743-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Voltaren (Novartis)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>166496</Austr>
				<PresentationName>Voltaren</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Diclofenac sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Voltaren</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcvltal10921</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>diclofenac sodium</ActiveIngredient>
						<ReleaseDate>2021-09-28 14:40:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/01/2011 13:12</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>BZ</Side1Marking>
							<Side2Marking>CG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>166496-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>37582</Austr>
				<PresentationName>Voltaren</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Suppositories</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Diclofenac sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Voltaren</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcvltal10921</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>diclofenac sodium</ActiveIngredient>
						<ReleaseDate>2021-09-28 14:40:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/12/2008 10:47</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Suppositories</DoseForm>
							<Colour>yellowish-white</Colour>
							<Scoring></Scoring>
							<Shape>torpedo</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>37582-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>42943</Austr>
				<PresentationName>Voltaren Rapid</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Diclofenac potassium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Voltaren Rapid</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcvlror10921</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>diclofenac potassium</ActiveIngredient>
						<ReleaseDate>2021-09-28 14:44:03.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>20/01/2009 10:33</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>reddish-brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>42943-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>66880</Austr>
				<PresentationName>Voltaren</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Diclofenac sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Voltaren</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcvltal10921</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>diclofenac sodium</ActiveIngredient>
						<ReleaseDate>2021-09-28 14:40:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>07/01/2011 13:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale brown</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>GT</Side1Marking>
							<Side2Marking>CG</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>66880-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>96797</Austr>
				<PresentationName>Voltaren</PresentationName>
    			<PresentionStrength>12.5mg</PresentionStrength>
    			<PresentationForm>Suppositories</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Diclofenac sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Voltaren</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcvltal10921</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>diclofenac sodium</ActiveIngredient>
						<ReleaseDate>2021-09-28 14:40:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/09/2008 13:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Suppositories</DoseForm>
							<Colour>yellowish-white</Colour>
							<Scoring></Scoring>
							<Shape>torpedo</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96797-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>96810</Austr>
				<PresentationName>Voltaren</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Suppositories</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Diclofenac sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Voltaren</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>nvcvltal10921</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>diclofenac sodium</ActiveIngredient>
						<ReleaseDate>2021-09-28 14:40:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/12/2008 10:46</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Suppositories</DoseForm>
							<Colour>yellowish-white</Colour>
							<Scoring></Scoring>
							<Shape>torpedo</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96810-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>96811</Austr>
				<PresentationName>Voltaren</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Suppositories</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Diclofenac sodium</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Voltaren</DocumentName>
						<DocumentTypes>
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						</DocumentTypes>
						<ActiveIngredient>diclofenac sodium</ActiveIngredient>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/12/2008 10:46</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Scoring></Scoring>
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							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>96811-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Voriconazole (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>218361</Austr>
				<PresentationName>Voriconazole Apotex</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Voriconazole</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
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							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>modified oval-shaped</Shape>
							<Side1Marking>VOR 200</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>218361-C01-01-BL600.jpg</ImageFileName>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>218362</Austr>
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    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Voriconazole</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateEffective>08/12/2016 10:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>VOR 50</Side1Marking>
							<Side2Marking>APO</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>218362-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>307466</Austr>
				<PresentationName>Voriconazole APO</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>V50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>307466-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>307467</Austr>
				<PresentationName>Voriconazole APO</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>V200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>307467-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Voriconazole (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>207785</Austr>
				<PresentationName>Voriconazole Sandoz</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>09/01/2018 17:10</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>200</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>207785-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>207786</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Voriconazole</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>50</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>207786-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Votrient</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>161281</Austr>
				<PresentationName>Votrient</PresentationName>
    			<PresentionStrength>400mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Pazopanib hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Votrient</DocumentName>
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							<DocumentType>eCMI</DocumentType>
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								<Format>PDF</Format>
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						<ActiveIngredient>pazopanib hydrochloride</ActiveIngredient>
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				</Documents>
				<Images>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified capsule-shaped</Shape>
							<Side1Marking>GS UHL</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>161281-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>161282</Austr>
				<PresentationName>Votrient</PresentationName>
    			<PresentionStrength>200mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Pazopanib hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Votrient</DocumentName>
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							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
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							<Shape>modified capsule-shaped</Shape>
							<Side1Marking>GS JT</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>161282-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Voxam</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>111781</Austr>
				<PresentationName>Voxam</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluvoxamine maleate</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>291 291</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>111782</Austr>
				<PresentationName>Voxam</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluvoxamine maleate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>23/10/2012 15:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>313 313</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>111782-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Vttack</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>206983</Austr>
				<PresentationName>Vttack</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Voriconazole</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Vttack</DocumentName>
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				<Images>
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                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
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							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
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							<Views>
							<View>
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					</Versions>
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			<Presentations>
				<Austr>206985</Austr>
				<PresentationName>Vttack</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentTypes>
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				<Images>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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		</Brand><Brand>
			<brandname>Vyndamax</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>314813</Austr>
				<PresentationName>Vyndamax</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>tafamidis</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<Views>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin,Ezetimibe</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Vytorin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcvytor11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ezetimibe with simvastatin</ActiveIngredient>
						<ReleaseDate>2022-10-20 19:23:15.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/01/2011 19:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>311</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>98100-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>98111</Austr>
				<PresentationName>Vytorin</PresentationName>
    			<PresentionStrength>10mg/20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ezetimibe,Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Vytorin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcvytor11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ezetimibe with simvastatin</ActiveIngredient>
						<ReleaseDate>2022-10-20 19:23:15.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/12/2008 13:22</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>312</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>98111-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>98115</Austr>
				<PresentationName>Vytorin</PresentationName>
    			<PresentionStrength>10mg/40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin,Ezetimibe</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Vytorin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcvytor11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ezetimibe with simvastatin</ActiveIngredient>
						<ReleaseDate>2022-10-20 19:23:15.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>02/12/2008 13:21</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>313</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>98115-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>98117</Austr>
				<PresentationName>Vytorin</PresentationName>
    			<PresentionStrength>10mg/80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin,Ezetimibe</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Vytorin</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqcvytor11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>ezetimibe with simvastatin</ActiveIngredient>
						<ReleaseDate>2022-10-20 19:23:15.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>09/03/2010 08:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>315</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>98117-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Vyvanse</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>199226</Austr>
				<PresentationName>Vyvanse</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Lisdexamfetamine dimesilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Vyvanse</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tkcvyvan11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lisdexamfetamine dimesilate</ActiveIngredient>
						<ReleaseDate>2022-10-19 13:13:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/09/2015 09:39</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue opaque and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>S489</Side1Marking>
							<Side2Marking>50 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199226-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199227</Austr>
				<PresentationName>Vyvanse</PresentationName>
    			<PresentionStrength>30mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Lisdexamfetamine dimesilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Vyvanse</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tkcvyvan11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lisdexamfetamine dimesilate</ActiveIngredient>
						<ReleaseDate>2022-10-19 13:13:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/09/2015 09:40</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>pink opaque and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>S489</Side1Marking>
							<Side2Marking>30 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199227-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>199228</Austr>
				<PresentationName>Vyvanse</PresentationName>
    			<PresentionStrength>70mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Lisdexamfetamine dimesilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Vyvanse</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tkcvyvan11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lisdexamfetamine dimesilate</ActiveIngredient>
						<ReleaseDate>2022-10-19 13:13:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/09/2015 09:41</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>pink opaque and blue opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>S489</Side1Marking>
							<Side2Marking>70 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>199228-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>284019</Austr>
				<PresentationName>Vyvanse</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Lisdexamfetamine dimesilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Vyvanse</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tkcvyvan11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lisdexamfetamine dimesilate</ActiveIngredient>
						<ReleaseDate>2022-10-19 13:13:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/08/2022 09:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>ivory opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>S489</Side1Marking>
							<Side2Marking>20 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>284019-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>284020</Austr>
				<PresentationName>Vyvanse</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Lisdexamfetamine dimesilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Vyvanse</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tkcvyvan11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lisdexamfetamine dimesilate</ActiveIngredient>
						<ReleaseDate>2022-10-19 13:13:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/08/2022 09:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue/green opaque and white opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>S489</Side1Marking>
							<Side2Marking>40 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>284020-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>284021</Austr>
				<PresentationName>Vyvanse</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Lisdexamfetamine dimesilate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Vyvanse</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>tkcvyvan11022</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lisdexamfetamine dimesilate</ActiveIngredient>
						<ReleaseDate>2022-10-19 13:13:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>24/08/2022 09:09</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>aqua blue opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>S489</Side1Marking>
							<Side2Marking>60 mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>284021-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Xarelto</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>147400</Austr>
				<PresentationName>Xarelto</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2011 14:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Triangle 10</Side1Marking>
							<Side2Marking>Bayer Cross</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>147400-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>181185</Austr>
				<PresentationName>Xarelto</PresentationName>
    			<PresentionStrength>15mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/06/2012 15:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Triangle 15</Side1Marking>
							<Side2Marking>Bayer Cross</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>181185-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>181186</Austr>
				<PresentationName>Xarelto</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>14/06/2012 15:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brown-red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Triangle 20</Side1Marking>
							<Side2Marking>Bayer Cross</Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>181186-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Xatral SR</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>81900</Austr>
				<PresentationName>Xatral SR</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Alfuzosin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Xatral SR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>swcxatra21120</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>alfuzosin hydrochloride</ActiveIngredient>
						<ReleaseDate>2020-12-22 15:14:31.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/02/2010 14:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow and white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>81900-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Xelabine</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>213045</Austr>
				<PresentationName>Xelabine</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets </PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>capecitabine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Xelabine</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>gocxelbn10622</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>capecitabine</ActiveIngredient>
						<ReleaseDate>2022-07-01 16:01:29.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>31/01/2022 16:01</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>213045-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Xelevia</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>220107</Austr>
				<PresentationName>Xelevia</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sitagliptin phosphate monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Xelevia</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>mkcxelev10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>Sitagliptin phosphate monohydrate</ActiveIngredient>
						<ReleaseDate>2022-07-08 15:10:16.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>02/12/2022 08:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>277</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>220107-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>220108</Austr>
				<PresentationName>Xelevia</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sitagliptin phosphate monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Xelevia</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>mkcxelev10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>Sitagliptin phosphate monohydrate</ActiveIngredient>
						<ReleaseDate>2022-07-08 15:10:16.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>02/12/2022 08:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light beige</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>112</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>220108-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>220109</Austr>
				<PresentationName>Xelevia</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sitagliptin phosphate monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Xelevia</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>mkcxelev10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>Sitagliptin phosphate monohydrate</ActiveIngredient>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>02/12/2022 08:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>221</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>220109-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Xeljanz</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>196987</Austr>
				<PresentationName>Xeljanz</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Tofacitinib citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Xeljanz</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcxeljt11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tofacitinib citrate</ActiveIngredient>
						<ReleaseDate>2021-10-18 13:53:46.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>29/02/2016 09:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>JKI 5</Side1Marking>
							<Side2Marking>Pfizer</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>196987-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>298307</Austr>
				<PresentationName>Xeljanz</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>tofacitinib citrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Xeljanz</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfcxeljt11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tofacitinib citrate</ActiveIngredient>
						<ReleaseDate>2021-10-18 13:53:46.0</ReleaseDate>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/04/2019 14:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>blue</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>JKI 10</Side1Marking>
							<Side2Marking>Pfizer</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>298307-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Xenical</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>61598</Austr>
				<PresentationName>Xenical</PresentationName>
    			<PresentionStrength>120mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 15:11</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>turquoise</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>ROCHE</Side1Marking>
							<Side2Marking>XENICAL 120</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>61598-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Xergic</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>115377</Austr>
				<PresentationName>Xergic</PresentationName>
    			<PresentionStrength>120mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>115377-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>115378</Austr>
				<PresentationName>Xergic</PresentationName>
    			<PresentionStrength>180mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>23/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>115378-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Xigduo XR</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>211294</Austr>
				<PresentationName>Xigduo XR</PresentationName>
    			<PresentionStrength>10mg/500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Metformin hydrochloride,Dapagliflozin propanediol monohydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Xigduo XR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
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						<ActiveIngredient>dapagliflozin propanediol monohydrate with metformin hydrochloride</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/03/2016 14:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>1072 10/500</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>211294-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>211295</Austr>
				<PresentationName>Xigduo XR</PresentationName>
    			<PresentionStrength>10mg/1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Dapagliflozin propanediol monohydrate,Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Xigduo XR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>apcxigdu10922</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>dapagliflozin propanediol monohydrate with metformin hydrochloride</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/03/2016 14:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow to dark yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>1073 10/1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>211295-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>211296</Austr>
				<PresentationName>Xigduo XR</PresentationName>
    			<PresentionStrength>5mg/1000mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Dapagliflozin propanediol monohydrate,Metformin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Xigduo XR</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>03/03/2016 14:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink to dark pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>1071 5/1000</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>211296-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Xtandi</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>210494</Austr>
				<PresentationName>Xtandi</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>enzalutamide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Xtandi</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2015 12:18</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring></Scoring>
							<Shape>oblong</Shape>
							<Side1Marking>ENZ</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>210494-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Xyvion</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>132518</Austr>
				<PresentationName>Xyvion</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Tibolone</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Xyvion</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>tibolone</ActiveIngredient>
						<ReleaseDate>2021-04-30 11:18:09.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>13/10/2011 14:51</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>MK 2</Side1Marking>
							<Side2Marking>ORGANON *</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>132518-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Yasmin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>77039</Austr>
				<PresentationName>Yasmin</PresentationName>
    			<PresentionStrength>*</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>05/05/2010 15:50</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DO hexagon</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>77039-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DP hexagon</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>77039-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Yaz</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>133649</Austr>
				<PresentationName>Yaz</PresentationName>
    			<PresentionStrength>20mcg/3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/04/2010 16:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DP hexagon</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133649-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DS hexagon</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>133649-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>179878</Austr>
				<PresentationName>Yaz Flex</PresentationName>
    			<PresentionStrength>20mcg/3mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>dial dispenser pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/06/2012 13:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>DS hexagon</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>179878-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zabep</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>191867</Austr>
				<PresentationName>Zabep</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zabep</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afczabep11214</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>rabeprazole sodium</ActiveIngredient>
						<ReleaseDate>2015-03-03 15:13:45.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>07/11/2016 15:55</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>elliptical</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>191867-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zactin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>53773</Austr>
				<PresentationName>Zactin Caps</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zactin Caps</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afczactc11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fluoxetine hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-10-05 14:24:40.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/03/2014 10:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>light purple opaque and light green opaque</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>&#945;</Side1Marking>
							<Side2Marking>FL 20</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>53773-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>90913</Austr>
				<PresentationName>Zactin Tabs</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Fluoxetine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zactin Tabs</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afczactt11021</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>fluoxetine hydrochloride</ActiveIngredient>
						<ReleaseDate>2021-10-05 14:24:51.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>05/06/2012 13:48</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>FL 20</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>90913-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zan-Extra</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>120955</Austr>
				<PresentationName>Zan-Extra</PresentationName>
    			<PresentionStrength>10mg/10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Enalapril maleate,Lercanidipine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zan-Extra</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goczanex10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lercanidipine hydrochloride with enalapril maleate</ActiveIngredient>
						<ReleaseDate>2022-02-04 12:28:52.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/09/2008 15:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>120955-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>120961</Austr>
				<PresentationName>Zan-Extra</PresentationName>
    			<PresentionStrength>10mg/20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Enalapril maleate,Lercanidipine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zan-Extra</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goczanex10222</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lercanidipine hydrochloride with enalapril maleate</ActiveIngredient>
						<ReleaseDate>2022-02-04 12:28:52.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/09/2008 15:26</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>circular</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>120961-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zanidip</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>77506</Austr>
				<PresentationName>Zanidip</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lercanidipine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zanidip</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goczanid20322</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lercanidipine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-03-14 07:52:23.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>30/09/2008 15:29</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>77506-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>93733</Austr>
				<PresentationName>Zanidip</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lercanidipine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
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						<DocumentTypes>
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								<Format>PDF</Format>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
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			</Presentations>
		</Brand><Brand>
			<brandname>Zantac</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>45993</Austr>
				<PresentationName>Zantac Effervescent Tablets</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>tube</Container>
    			<TGAIngredient>Ranitidine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Colour>white to pale yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>GS LHK</Side1Marking>
							<Side2Marking></Side2Marking>
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			<Presentations>
				<Austr>53323</Austr>
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    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient>Ranitidine hydrochloride</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>GX EC3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>53323-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>53324</Austr>
				<PresentationName>Zantac Tablets</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ranitidine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>GX EC2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>53324-C01-01-BL600.jpg</ImageFileName>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zantac (GSK CHC)</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>71786</Austr>
				<PresentationName>Zantac 12hr Action</PresentationName>
    			<PresentionStrength>150mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>GX EC2</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
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								<ImageFileName>71786-C01-01-BL600.jpg</ImageFileName>
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			<Presentations>
				<Austr>95076</Austr>
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    			<PresentionStrength>300mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Side1Marking>GX EC3</Side1Marking>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>94175</Austr>
				<PresentationName>Zarontin</PresentationName>
    			<PresentionStrength>250mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Ethosuximide</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<QualiferData></QualiferData>
						<DocumentName>Zarontin</DocumentName>
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						<DateEffective>04/10/2011 16:24</DateEffective>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Shape></Shape>
							<Side1Marking>P-D 237</Side1Marking>
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							<Views>
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		</Brand><Brand>
			<brandname>Zavedos</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>73516</Austr>
				<PresentationName>Zavedos </PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-02-02 00:00:00'}</WithdrawalDate>
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    			<TGAIngredient>Idarubicin hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Shape></Shape>
							<Side1Marking>IDARUBICIN 5</Side1Marking>
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							<Views>
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			</Presentations>
			<Presentations>
				<Austr>73517</Austr>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate>{ts '2022-02-02 00:00:00'}</WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>IDARUBICIN 10</Side1Marking>
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							<Views>
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			</Presentations>
		</Brand><Brand>
			<brandname>Zedace</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>57369</Austr>
				<PresentationName>Zedace</PresentationName>
    			<PresentionStrength>12.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Captopril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateEffective>24/03/2010 15:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<Shape>elongated</Shape>
							<Side1Marking>C12.5</Side1Marking>
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			</Presentations>
			<Presentations>
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				<PresentationName>Zedace</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container></Container>
    			<TGAIngredient>Captopril</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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   				<WithdrawalDate></WithdrawalDate>
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							<Side1Marking>CT 50</Side1Marking>
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			<brandname>Zedd</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>107602</Austr>
				<PresentationName>Zedd</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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							<Side1Marking>AT 500</Side1Marking>
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							<Views>
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		</Brand><Brand>
			<brandname>Zeffix</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>66828</Austr>
				<PresentationName>Zeffix</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lamivudine</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Side1Marking>GX CG5</Side1Marking>
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							<Views>
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			</Presentations>
		</Brand><Brand>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>232437</Austr>
				<PresentationName>Zeklen</PresentationName>
    			<PresentionStrength>10mg/20mg</PresentionStrength>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>183674</Austr>
				<PresentationName>Zelboraf</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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		</Brand><Brand>
			<brandname>Zeldox</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>65526</Austr>
				<PresentationName>Zeldox</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<IsAMasterPack>No</IsAMasterPack>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
				<Austr>43928</Austr>
				<PresentationName>Zentel</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
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							<Shape>round</Shape>
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							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>70837-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>70838</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lisinopril</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
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						<ActiveIngredient>lisinopril dihydrate</ActiveIngredient>
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				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/06/2011 10:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
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							<Side1Marking>Heart image 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>70839</Austr>
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    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
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				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/06/2011 10:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brownish-red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>Heart image 20</Side1Marking>
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							<View>
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							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zetin</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>196004</Austr>
				<PresentationName>Zetin</PresentationName>
    			<PresentionStrength>25mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>22/10/2018 14:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>brown and yellow to light yellow</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>A25</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>196004-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>196005</Austr>
				<PresentationName>Zetin</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>brown and white to off-white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>A10</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>196005-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zetlam</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>180504</Austr>
				<PresentationName>Zetlam</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zetlam</DocumentName>
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						<VersionSequence>1</VersionSequence>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
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							<Side1Marking>LN1</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ziagen</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>66878</Austr>
				<PresentationName>Ziagen Tablets</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DocumentName>Ziagen Tablets</DocumentName>
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						<ActiveIngredient>abacavir sulfate</ActiveIngredient>
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							<PhaseItem>1</PhaseItem>
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							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>GX 623</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zient</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>232497</Austr>
				<PresentationName>Zient</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ezetimibe</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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							<AvailableFormats>
								<Format>PDF</Format>
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						<ActiveIngredient>ezetimibe</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>25/06/2019 15:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>414</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>232497-C01-01-BL600.jpg</ImageFileName>
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							</Views>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zilarex</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>120710</Austr>
				<PresentationName>Zilarex 10mg Tablets</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>29/09/2008 13:24</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>120710-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zimstat</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>95672</Austr>
				<PresentationName>Zimstat</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Zimstat</DocumentName>
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						<ActiveIngredient>simvastatin</ActiveIngredient>
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				<Images>
					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark buff</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SM 5</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>95672-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>95673</Austr>
				<PresentationName>Zimstat</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
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						<DocumentName>Zimstat</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>simvastatin</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark peach to pink</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SM 10</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>95673-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>95674</Austr>
				<PresentationName>Zimstat</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zimstat</DocumentName>
						<DocumentTypes>
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							<AvailableFormats>
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							</AvailableFormats>
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						<ActiveIngredient>simvastatin</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>dark tan</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SM 20</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>95674-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>95675</Austr>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zimstat</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
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							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>simvastatin</ActiveIngredient>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>24/06/2008 00:00</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>SM 40</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>95675-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>95676</Austr>
				<PresentationName>Zimstat</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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			<Presentations>
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			<Presentations>
				<Austr>95679</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
				<Austr>95680</Austr>
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   				<WithdrawalDate></WithdrawalDate>
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			<Presentations>
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			<brandname>Zincaps</brandname>
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			<Presentations>
				<Austr>27995</Austr>
				<PresentationName>Zincaps</PresentationName>
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							<View>
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			<Presentations>
				<Austr>47621</Austr>
				<PresentationName>Zinnat</PresentationName>
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					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/09/2014 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white/white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>CL64</Side1Marking>
							<Side2Marking>60mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>201059-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>201060</Austr>
				<PresentationName>APO-Ziprasidone</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ziprasidone hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>10/09/2014 11:06</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue/white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>CL65</Side1Marking>
							<Side2Marking>80mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>201060-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Ziprox</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>201081</Austr>
				<PresentationName>Ziprox</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/10/2018 14:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>CL62</Side1Marking>
							<Side2Marking>20mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>201081-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>201082</Austr>
				<PresentationName>Ziprox</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/10/2018 14:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>CL63</Side1Marking>
							<Side2Marking>40mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>201082-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>201083</Austr>
				<PresentationName>Ziprox</PresentationName>
    			<PresentionStrength>60mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/10/2018 14:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>CL64</Side1Marking>
							<Side2Marking>60mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>201083-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>201084</Austr>
				<PresentationName>Ziprox</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/10/2018 14:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>blue and white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking>CL65</Side1Marking>
							<Side2Marking>80mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>201084-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zircol</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>295935</Austr>
				<PresentationName>Zircol</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lercanidipine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zircol 10 and Zircol 20</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afczircl10322</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lercanidipine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-03-14 07:51:33.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/12/2018 11:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>scored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>295935-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>295936</Austr>
				<PresentationName>Zircol</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Lercanidipine hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zircol 10 and Zircol 20</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>afczircl10322</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>lercanidipine hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-03-14 07:51:33.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/12/2018 11:34</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>295936-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zithro</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>241812</Austr>
				<PresentationName>Zithro</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>22/10/2018 14:07</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oblong</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>241812-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zithromax</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>58797</Austr>
				<PresentationName>Zithromax</PresentationName>
    			<PresentionStrength>500mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Azithromycin dihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zithromax</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfczithb10122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>azithromycin dihydrate</ActiveIngredient>
						<ReleaseDate>2022-01-27 15:50:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>2</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>19/09/2019 07:23</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white to off-white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>modified capsule-shaped</Shape>
							<Side1Marking>ZTM 500</Side1Marking>
							<Side2Marking>Pfizer</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>58797-C01-02-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>60057</Austr>
				<PresentationName>Zithromax</PresentationName>
    			<PresentionStrength>600mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Azithromycin dihydrate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zithromax</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>pfczithb10122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>azithromycin dihydrate</ActiveIngredient>
						<ReleaseDate>2022-01-27 15:50:57.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/09/2008 16:17</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>ZTM 600</Side1Marking>
							<Side2Marking>Pfizer</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>60057-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zocor</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>39917</Austr>
				<PresentationName>Zocor</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zocor</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqczocor10221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>simvastatin</ActiveIngredient>
						<ReleaseDate>2021-04-30 11:21:59.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>17/11/2008 18:02</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>buff</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>ZOCOR 5</Side1Marking>
							<Side2Marking>MSD 726</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>39917-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>58864</Austr>
				<PresentationName>Zocor</PresentationName>
    			<PresentionStrength>40mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zocor</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqczocor10221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>simvastatin</ActiveIngredient>
						<ReleaseDate>2021-04-30 11:21:59.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 12:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brick-red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MSD 749</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>58864-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>65975</Austr>
				<PresentationName>Zocor</PresentationName>
    			<PresentionStrength>20mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zocor</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqczocor10221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>simvastatin</ActiveIngredient>
						<ReleaseDate>2021-04-30 11:21:59.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 12:45</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>tan</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MSD 740</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>65975-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>65976</Austr>
				<PresentationName>Zocor</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zocor</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqczocor10221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>simvastatin</ActiveIngredient>
						<ReleaseDate>2021-04-30 11:21:59.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>17/11/2008 18:03</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>peach</Colour>
							<Scoring></Scoring>
							<Shape>oval</Shape>
							<Side1Marking>MSD 735</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>65976-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>65977</Austr>
				<PresentationName>Zocor</PresentationName>
    			<PresentionStrength>80mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Simvastatin</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zocor</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>oqczocor10221</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>simvastatin</ActiveIngredient>
						<ReleaseDate>2021-04-30 11:21:59.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>26/09/2008 12:44</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>brick-red</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>543</Side1Marking>
							<Side2Marking>80</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>65977-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zoely</brandname>
			<isamtbrand>false</isamtbrand>
			<Presentations>
				<Austr>168332</Austr>
				<PresentationName>Zoely</PresentationName>
    			<PresentionStrength>2.5mg/1.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Oestradiol hemihydrate,Nomegestrol acetate</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zoely</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>ttczoely10722</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>nomegestrol acetate with estradiol</ActiveIngredient>
						<ReleaseDate>2022-07-22 11:08:36.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>18/05/2012 14:54</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>ne</Side1Marking>
							<Side2Marking>ne</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>168332-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
							<PhaseItem>2</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>p</Side1Marking>
							<Side2Marking>p</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>168332-C02-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zofran</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>60801</Austr>
				<PresentationName>Zofran Suppositories</PresentationName>
    			<PresentionStrength>16mg</PresentionStrength>
    			<PresentationForm>Suppositories</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ondansetron</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 16:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Suppositories</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape>torpedo</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>60801-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>63054</Austr>
				<PresentationName>Zofran Zydis Wafers</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Wafers</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ondansetron</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 16:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Wafers</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>63054-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>63055</Austr>
				<PresentationName>Zofran Zydis Wafers</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Wafers</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ondansetron</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>15/10/2008 14:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Wafers</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>63055-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>9979</Austr>
				<PresentationName>Zofran Tablets</PresentationName>
    			<PresentionStrength>4mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ondansetron hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>29/08/2008 16:36</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>GX ET3</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>9979-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>9981</Austr>
				<PresentationName>Zofran Tablets</PresentationName>
    			<PresentionStrength>8mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ondansetron hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>14/08/2008 15:49</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>yellow</Colour>
							<Scoring>unscored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>GX ET5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>9981-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zolinza</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>156430</Austr>
				<PresentationName>Zolinza</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
    			<TGAIngredient>Vorinostat</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zolinza</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>mkczolin11220</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>vorinostat</ActiveIngredient>
						<ReleaseDate>2021-01-05 14:34:04.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>11/08/2014 14:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>white</Colour>
							<Scoring></Scoring>
							<Shape></Shape>
							<Side1Marking></Side1Marking>
							<Side2Marking>568 100mg</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>156430-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zolmitriptan (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>200878</Austr>
				<PresentationName>APO-Zolmitriptan</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Zolmitriptan</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>06/01/2016 14:53</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>light pink</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>2.5</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>200878-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zoloft</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>321601</Austr>
				<PresentationName>Zoloft</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>sertraline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
						<DocumentName>Zoloft</DocumentName>
						<DocumentTypes>
							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
								<Format>PDF</Format>
								<Filename>goczolot21122</Filename>
							</AvailableFormats>
						</DocumentTypes>
						<ActiveIngredient>sertraline hydrochloride</ActiveIngredient>
						<ReleaseDate>2022-12-02 09:20:10.0</ReleaseDate>
					</DocumentQualifiers>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>20/05/2022 13:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>ZLT 50</Side1Marking>
							<Side2Marking>Pfizer</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>321601-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>42950</Austr>
				<PresentationName>Zoloft</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sertraline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>04/10/2011 16:28</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>ZLT-100</Side1Marking>
							<Side2Marking>Pfizer</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>42950-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>42979</Austr>
				<PresentationName>Zoloft</PresentationName>
    			<PresentionStrength>50mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Sertraline hydrochloride</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>03/09/2008 16:19</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>capsule-shaped</Shape>
							<Side1Marking>ZLT 50</Side1Marking>
							<Side2Marking>Pfizer</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>42979-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zolpidem (Amneal)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>131917</Austr>
				<PresentationName>Zolpidem AN</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
				</Documents>
				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>Current</VersionStatus>
						<DateEffective>13/03/2019 14:35</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>ZIM 10</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>131917-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zolpidem Tartrate (Apotex)</brandname>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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				<Austr>119091</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<brandname>Zolpidem Tartrate (Generic Health)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>119087</Austr>
				<PresentationName>Zolpibell</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>ZIM 10</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>119087-C01-01-BL600.jpg</ImageFileName>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zolpidem Tartrate (Pharmacor)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>131918</Austr>
				<PresentationName>Zolpidem (Pharmacor)</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>scored</Scoring>
							<Shape>oval</Shape>
							<Side1Marking>ZIM 10</Side1Marking>
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			</Presentations>
		</Brand><Brand>
			<brandname>Zolpidem Tartrate (Sandoz)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>128095</Austr>
				<PresentationName>Zolpidem Sandoz</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<QualiferData></QualiferData>
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							<AvailableFormats>
								<Format>PDF</Format>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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		</Brand><Brand>
			<brandname>Zoltrip</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>200877</Austr>
				<PresentationName>Zoltrip</PresentationName>
    			<PresentionStrength>2.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient></TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			</Presentations>
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			<brandname>Zomig</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>61325</Austr>
				<PresentationName>Zomig</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zonisamide (Apotex)</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>265574</Austr>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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							<Shape></Shape>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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			<brandname>Zopiclone (Apotex)</brandname>
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			<Presentations>
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			<isamtbrand>true</isamtbrand>
			<Presentations>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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				<Images>
					<Versions>
						<VersionSequence>1</VersionSequence>
						<VersionStatus>current</VersionStatus>
						<DateEffective>16/12/2008 10:04</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>T1</Side1Marking>
							<Side2Marking>Grunenthal logo</Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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			<Presentations>
				<Austr>80725</Austr>
				<PresentationName>Zydol SR</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>deep orange to brown</Colour>
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							<Side1Marking>T3</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>80726</Austr>
				<PresentationName>Zydol SR</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<Versions>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>pale orange</Colour>
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							<Shape>round</Shape>
							<Side1Marking>T2</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>80726-C01-01-BL600.jpg</ImageFileName>
							</View>
							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
		</Brand><Brand>
			<brandname>Zykadia</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>235737</Austr>
				<PresentationName>Zykadia</PresentationName>
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    			<PresentationForm>Capsules</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Ceritinib</TGAIngredient>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
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								<Format>PDF</Format>
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						<VersionSequence>1</VersionSequence>
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						<DateEffective>16/10/2017 10:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer>1</DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Capsules</DoseForm>
							<Colour>opaque blue and opaque white</Colour>
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							<Shape></Shape>
							<Side1Marking>LDK 150MG</Side1Marking>
							<Side2Marking>NVR</Side2Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
		</Brand><Brand>
			<brandname>Zyloprim</brandname>
			<isamtbrand>true</isamtbrand>
			<Presentations>
				<Austr>286086</Austr>
				<PresentationName>Zyloprim</PresentationName>
    			<PresentionStrength>100mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>bottle</Container>
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					<Versions>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
							<Side1Marking>AP 100</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>286087</Austr>
				<PresentationName>Zyloprim</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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					<Versions>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Shape>round</Shape>
							<Side1Marking>AP 300</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
		</Brand><Brand>
			<brandname>Zypine</brandname>
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			<Presentations>
				<Austr>154617</Austr>
				<PresentationName>Zypine</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
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				<Documents>
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							<PhaseItem>1</PhaseItem>
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							<Side1Marking>OZ 10</Side1Marking>
							<Side2Marking>G</Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>154620</Austr>
				<PresentationName>Zypine</PresentationName>
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    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
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				<Documents>
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						<ActiveIngredient>olanzapine</ActiveIngredient>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Side1Marking>OZ 2.5</Side1Marking>
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							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>154621</Austr>
				<PresentationName>Zypine</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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						</DocumentTypes>
						<ActiveIngredient>olanzapine</ActiveIngredient>
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				<Images>
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						<VersionSequence>1</VersionSequence>
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                    	<Phase>
							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>OZ 7.5</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			</Presentations>
			<Presentations>
				<Austr>154624</Austr>
				<PresentationName>Zypine</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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							<PhaseItem>1</PhaseItem>
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							<Side1Marking>OZ 5</Side1Marking>
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							<View>
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					</Versions>
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			</Presentations>
			<Presentations>
				<Austr>175773</Austr>
				<PresentationName>Zypine ODT</PresentationName>
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    			<PresentationForm>Wafers</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Wafers</DoseForm>
							<Colour>light yellow to yellow, plain to mottled</Colour>
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							<Shape>round</Shape>
							<Side1Marking>OE1</Side1Marking>
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							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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			<Presentations>
				<Austr>175775</Austr>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
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    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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			<Presentations>
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			<brandname>Zyprexa</brandname>
			<isamtbrand>true</isamtbrand>
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				<Austr>56603</Austr>
				<PresentationName>Zyprexa</PresentationName>
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   				<WithdrawalDate></WithdrawalDate>
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							<View>
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			</Presentations>
			<Presentations>
				<Austr>56604</Austr>
				<PresentationName>Zyprexa</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>LILLY 4115</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
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						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>56605</Austr>
				<PresentationName>Zyprexa</PresentationName>
    			<PresentionStrength>7.5mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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					<DocumentQualifiers>
						<QualifierType></QualifierType>
						<QualiferData></QualiferData>
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						<ActiveIngredient>olanzapine</ActiveIngredient>
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					<Versions>
						<VersionSequence>1</VersionSequence>
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						<DateEffective>29/09/2008 09:42</DateEffective>
						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
							<Colour>white</Colour>
							<Scoring>unscored</Scoring>
							<Shape>round</Shape>
							<Side1Marking>LILLY 4116</Side1Marking>
							<Side2Marking></Side2Marking>
							<Views>
							<View>
								<ViewLabel>C</ViewLabel>
								<ImageFileName>56605-C01-01-BL600.jpg</ImageFileName>
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							</Views>
						</Phase>
					</Versions>
				</Images>
			</Presentations>
			<Presentations>
				<Austr>56606</Austr>
				<PresentationName>Zyprexa</PresentationName>
    			<PresentionStrength>10mg</PresentionStrength>
    			<PresentationForm>Tablets</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<DateVersionWithdrawn></DateVersionWithdrawn>
                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Tablets</DoseForm>
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							<Side1Marking>LILLY 4117</Side1Marking>
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							<View>
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			</Presentations>
			<Presentations>
				<Austr>73388</Austr>
				<PresentationName>Zyprexa Zydis</PresentationName>
    			<PresentionStrength>5mg</PresentionStrength>
    			<PresentationForm>Wafers</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
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						<ActiveIngredient>olanzapine</ActiveIngredient>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
							<DoseForm>Zydis Wafers</DoseForm>
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							<Side1Marking></Side1Marking>
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							<View>
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			</Presentations>
			<Presentations>
				<Austr>73389</Austr>
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    			<PresentationForm>Wafers</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
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						<DocumentName>Zyprexa; Zyprexa Zydis</DocumentName>
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						<ActiveIngredient>olanzapine</ActiveIngredient>
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                    	<DisplayMedicationDisclaimer></DisplayMedicationDisclaimer>
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							<PhaseItem>1</PhaseItem>
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			<Presentations>
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   				<WithdrawalDate></WithdrawalDate>
    			<Container>blister pack</Container>
    			<TGAIngredient>Olanzapine</TGAIngredient>
    			<IsAMasterPack>No</IsAMasterPack>
    			<IsASubpackOfAUSTR></IsASubpackOfAUSTR>
				<Documents>
					<DocumentQualifiers>
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						<DocumentName>Zyprexa; Zyprexa Zydis</DocumentName>
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							<DocumentType>eCMI</DocumentType>
							<AvailableFormats>
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						<ActiveIngredient>olanzapine</ActiveIngredient>
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			<Presentations>
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    			<PresentationForm>Wafers</PresentationForm>
   				<WithdrawalDate></WithdrawalDate>
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