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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

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Search

Sponsor content

348 result(s) found, displaying 231 to 240

TEMODAL temozolomide 20mg capsule bottle Cancelled under Section 30(1)(c) of the Act

28 June 2019

Cancellation by sponsor

Requested by Merck Sharp & Dohme (Australia) Pty Ltd
PREGNYL gonadotrophin - chorionic human 1500IU powder for injection ampoule with diluent ampoule Cancelled under Section 30(1)(c) of the Act

27 June 2019

Cancellation by sponsor

Requested by Merck Sharp & Dohme (Australia) Pty Ltd
PREGNYL gonadotrophin - chorionic human 5000IU powder for injection ampoule with diluent ampoule Cancelled under Section 30(1)(c) of the Act

27 June 2019

Cancellation by sponsor

Requested by Merck Sharp & Dohme (Australia) Pty Ltd
Notice for pembrolizumab (Merck Sharp & Dohme (Australia) Pty Ltd)

5 June 2019

Designation or determination

Provisional approval
KEYTRUDA (Merck Sharp & Dohme (Australia) Pty Ltd)

5 March 2019

Prescription medicine registration

Active ingredients: pembrolizumab.
NITRO-DUR 10 glyceryl trinitrate 80mg (10mg/24h) transdermal drug delivery system, sachet Cancelled under Section 30(1)(c) of the Act

4 February 2019

Cancellation by sponsor

Requested by Merck Sharp & Dohme (Australia) Pty Ltd
NITRO-DUR 15 glyceryl trinitrate 120mg (15mg/24h) Transdermal drug delivery system, sachet Cancelled under Section 30(1)(c) of the Act

4 February 2019

Cancellation by sponsor

Requested by Merck Sharp & Dohme (Australia) Pty Ltd
NITRO-DUR 5 glyceryl trinitrate 40mg (5mg/24h) transdermal drug delivery system, sachet Cancelled under Section 30(1)(c) of the Act

4 February 2019

Cancellation by sponsor

Requested by Merck Sharp & Dohme (Australia) Pty Ltd
NITRO-DUR 7.5 glyceryl trinitrate 60mg (7.5mg/24h) transdermal drug delivery system, sachet Cancelled under Section 30(1)(c) of the Act

4 February 2019

Cancellation by sponsor

Requested by Merck Sharp & Dohme (Australia) Pty Ltd
CRIXIVAN indinavir 200mg (as sulfate) capsule bottle Cancelled under Section 30(1)(c) of the Act

4 February 2019

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.