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Bristol-Myers Squibb Australia Pty Ltd

Regulatory activities for this sponsor.

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Type

ARTG (61)
Cancellation by sponsor (42)
Prescription medicine registration (34)
Australian public assessment report (AusPar) (33)
Designation or determination (5)
Prescription medicine decision summary (2)
Section 14, TGO91 consent (2)
Prescription medicine evaluation (1)

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Sponsor content

180 result(s) found, displaying 121 to 130

MONOPLUS 10/12.5 fosinopril 10mg and hydrochlorothiazide 12.5mg tablets bottle Cancelled under s30(1)(c) of the Act

5 April 2017

Cancellation by sponsor

Requested by Bristol-Myers Squibb Australia Pty Ltd
MONOPLUS 20/12.5 fosinopril 20mg and hydrochlorothiazide 12.5mg tablets blister pack Cancelled under s30(1)(c) of the Act

5 April 2017

Cancellation by sponsor

Requested by Bristol-Myers Squibb Australia Pty Ltd
MONOPLUS 20/12.5 fosinopril 20mg and hydrochlorothiazide 12.5mg tablets bottle Cancelled under s30(1)(c) of the Act

5 April 2017

Cancellation by sponsor

Requested by Bristol-Myers Squibb Australia Pty Ltd
MONOPLUS 10/12.5 fosinopril 10mg and hydrochlorothiazide 12.5mg tablets blister pack Cancelled under s30(1)(c)

5 April 2017

Cancellation by sponsor

Requested by Bristol-Myers Squibb Australia Pty Ltd
MONOPLUS 10/12.5 fosinopril 10mg and hydrochlorothiazide 12.5mg tablets bottle Cancelled under s30(1)(c)

5 April 2017

Cancellation by sponsor

Requested by Bristol-Myers Squibb Australia Pty Ltd
MONOPLUS 20/12.5 fosinopril 20mg and hydrochlorothiazide 12.5mg tablets blister pack Cancelled under s30(1)(c)

5 April 2017

Cancellation by sponsor

Requested by Bristol-Myers Squibb Australia Pty Ltd
MONOPLUS 20/12.5 fosinopril 20mg and hydrochlorothiazide 12.5mg tablets bottle Cancelled under s30(1)(c)

5 April 2017

Cancellation by sponsor

Requested by Bristol-Myers Squibb Australia Pty Ltd
AusPAR: Ipilimumab (rch)

23 February 2017

Australian public assessment report (AusPar)

Australian Public Assessment Report for Ipilimumab (rch)
Bristol-Myers Squibb Australia Pty Ltd - Organ preservation solution Cancelled under s41GL(d) of the Act

20 February 2017

Cancellation by sponsor

Requested by Bristol-Myers Squibb Australia Pty Ltd
Istodax (romidepsin) 10mg powder for injection vial, and solvent for reconstitution vial (198854)

7 August 2013

ARTG

Australian Register of Therapeutic Goods (ARTG) information for Istodax (romidepsin) 10mg powder for injection vial, and solvent for reconstitution vial.

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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.