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160 result(s) found, displaying 101 to 110
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 29/01/2021
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for MEDREICH BROMHEXINE CHESTY FORTE bromhexine hydrochloride 8 mg tablet blister pack.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for MEDREICH COLD RELIEF WITH COUGH capsule blister pack.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for MEDREICH PARACETAMOL PLUS CODEINE 500/9.6 paracetamol 500 mg and codeine phosphate hemihydrate 9.6 mg tablet blister pack.
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 28/01/2020
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 28/01/2020
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for DICLOFENAC AP 50 diclofenac sodium 50 mg modified release tablet blister pack.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for DICLOFENAC AP 25 diclofenac sodium 25 mg modified release tablet blister pack.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for DICLOFENAC TW 50 diclofenac sodium 50 mg modified release tablet blister pack.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for DICLOFENAC TW 25 diclofenac sodium 25 mg modified release tablet blister pack.