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AbbVie Pty Ltd

Regulatory activities for this sponsor.

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Type

ARTG (146)
Cancellation by sponsor (90)
Prescription medicine registration (26)
Australian public assessment report (AusPar) (22)
Designation or determination (7)
Prescription medicine evaluation (6)
Prescription medicine decision summary (2)
Section 14, TGO91 consent (1)

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2026 (7)
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Search

Sponsor content

300 result(s) found, displaying 61 to 70

Abbvie Pty Ltd - Tissue reconstructive material, biological Cancelled under Section 41GL(d) of the Act

28 June 2024

Cancellation by sponsor

Requested by Abbvie Pty Ltd
Abbvie Pty Ltd - Tissue reconstructive material, biological Cancelled under Section 41GL(d) of the Act

28 June 2024

Cancellation by sponsor

Requested by Abbvie Pty Ltd
Allergan Australia Pty Limited - Tissue reconstructive material, biological Cancelled under Section 41GL(d) of the Act

28 June 2024

Cancellation by sponsor

Requested by Abbvie Pty Ltd
Allergan Australia Pty Limited - Tissue reconstructive material, biological Cancelled under Section 41GL(d) of the Act

28 June 2024

Cancellation by sponsor

Requested by Abbvie Pty Ltd
AusPAR: Aquipta

27 June 2024

Australian public assessment report (AusPar)

Aquipta (atogepant) has been approved for the prophylaxis of migraine in adults who have at least four migraine days per month
RESTASIS (407824)

18 April 2023

ARTG

Australian Register of Therapeutic Goods (ARTG) information for RESTASIS.
VYALEV (Abbvie Pty Ltd)

4 March 2024

Prescription medicine registration

Active ingredients: foscarbidopa, foslevodopa.
EPKINLY (Abbvie Pty Ltd)

19 February 2024

Prescription medicine registration

Active ingredients: epcoritamab.
GENOPTIC gentamicin 3mg/mL (as sulfate) eye drops bottle Cancelled under Section 30(1)(c) of the Act

12 December 2023

Cancellation by sponsor

Requested by Abbvie Pty Ltd
OCUFEN flurbiprofen sodium dihydrate 0.03% eye drops, bottle Cancelled under Section 30(1)(c) of the Act

12 December 2023

Cancellation by sponsor

Requested by Abbvie Pty Ltd

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