Type
- Cancellation by sponsor (525)
- ARTG (454)
- Australian Public Assessment Report (AusPAR) (69)
- Prescription medicine registration (44)
- Section 14, TGO91 consent (21)
- Prescription medicine decision summary (19)
- Designation or determination (9)
- Cancellation or suspension (7)
- Prescription medicine evaluation (3)
Date
- 2026 (12)
- 2025 (44)
- 2024 (86)
- 2023 (73)
- 2022 (59)
- 2021 (124)
- 2020 (107)
- 2019 (98)
- 2018 (95)
- 2017 (73)
- 2016 (12)
- 2015 (22)
- 2014 (19)
- 2013 (9)
- 2012 (8)
- 2011 (14)
- 2010 (27)
- 2009 (13)
- 2008 (5)
- 2007 (11)
- 2006 (8)
- 2005 (4)
- 2004 (8)
- 2003 (3)
- 2002 (10)
- 2001 (6)
- 2000 (20)
- 1999 (9)
- 1998 (10)
- 1997 (16)
- 1996 (6)
- 1995 (3)
- 1994 (31)
- 1993 (16)
- 1992 (5)
- 1991 (85)
Sponsor content
1151 result(s) found, displaying 501 to 510
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Cancellation by sponsorRequested by Pfizer Australia Pty Ltd
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Cancellation by sponsorRequested by Pfizer Australia Pty Ltd
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Cancellation by sponsorRequested by Pfizer Australia Pty Ltd
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for DBL BORTEZOMIB 3.0 mg powder for injection vial.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for DBL BORTEZOMIB 3.5 mg powder for injection vial.
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ARTGAustralian Register of Therapeutic Goods (ARTG) information for DBL BORTEZOMIB 2.5 mg powder for injection vial.
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 8(f) of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 22/06/2020
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 8(f) of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 19/06/2020
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 8(f) of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 19/06/2020
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 8(f) of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 19/06/2020