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Merck Sharp & Dohme (Australia) Pty Ltd

Regulatory activities for this sponsor.

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Type

Cancellation by sponsor (138)
ARTG (79)
Prescription medicine registration (61)
Australian public assessment report (AusPar) (33)
Designation or determination (31)
Prescription medicine evaluation (4)
Prescription medicine decision summary (2)

Date

2025 (35)
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Search

Sponsor content

348 result(s) found, displaying 11 to 20

JANUVIA sitagliptin 25mg (as phosphate monohydrate) tablet blister pack Cancelled under Section 30(1)(c) of the Act

28 May 2025

Cancellation by sponsor

Requested by Merck Sharp & Dohme (Australia) Pty Ltd
JANUVIA sitagliptin 50mg (as phosphate monohydrate) tablet blister pack Cancelled under Section 30(1)(c) of the Act

28 May 2025

Cancellation by sponsor

Requested by Merck Sharp & Dohme (Australia) Pty Ltd
XELEVIA sitagliptin (as phosphate monohydrate) 100 mg film-coated tablet blister pack Cancelled under Section 30(1)(c) of the Act

28 May 2025

Cancellation by sponsor

Requested by Merck Sharp & Dohme (Australia) Pty Ltd
XELEVIA sitagliptin (as phosphate monohydrate) 50 mg film-coated tablet blister pack Cancelled under Section 30(1)(c) of the Act

28 May 2025

Cancellation by sponsor

Requested by Merck Sharp & Dohme (Australia) Pty Ltd
XELEVIA sitagliptin (as phosphate monohydrate) 25 mg film-coated tablet blister pack Cancelled under Section 30(1)(c) of the Act

28 May 2025

Cancellation by sponsor

Requested by Merck Sharp & Dohme (Australia) Pty Ltd
WELIREG (Merck Sharp & Dohme (Australia) Pty Ltd)

21 May 2025

Prescription medicine registration

Active ingredients: belzutifan.
ESMERON rocuronium bromide 50 mg/5 mL injection vial Cancelled under Section 30(1)(c) of the Act

12 May 2025

Cancellation by sponsor

Requested by Merck Sharp & Dohme (Australia) Pty Ltd
Merck Sharp & Dohme (Australia) Pty Ltd - Prefilled syringe/needle (471089)

29 November 2024

ARTG

Australian Register of Therapeutic Goods (ARTG) information for Merck Sharp & Dohme (Australia) Pty Ltd - Prefilled syringe/needle.
BRIDION sugammadex 500 mg/5 mL solution for injection vial Cancelled under Section 30(1)(c) of the Act

9 April 2025

Cancellation by sponsor

Requested by Merck Sharp & Dohme (Australia) Pty Ltd
BRIDION sugammadex 200 mg/2 mL solution for injection vial Cancelled under Section 30(1)(c) of the Act

9 April 2025

Cancellation by sponsor

Requested by Merck Sharp & Dohme (Australia) Pty Ltd

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The Department of Health, Disability and Ageing acknowledges First Nations peoples as the Traditional Owners of Country throughout Australia, and their continuing connection to land, sea and community. We pay our respects to them and their cultures, and to all Elders both past and present.