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Lundbeck Australia Pty Ltd

Regulatory activities for this sponsor.

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Type

ARTG (30)
Australian public assessment report (AusPar) (6)
Cancellation by sponsor (5)
Section 14, TGO91 consent (3)
Prescription medicine registration (2)

Date

2025 (2)
2024 (1)
2022 (1)
2021 (3)
2020 (3)
2019 (4)
2018 (3)
2017 (7)
2016 (1)
2014 (8)
2012 (1)
2011 (1)
2009 (1)
2003 (2)
1997 (1)
1994 (3)
1993 (4)

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Sponsor content

46 result(s) found, displaying 11 to 20

CON-TGO91-276 - Lundbeck Australia Pty Ltd

4 September 2020

Section 14, TGO91 consent

Product(s) approved for Supply with noncompliant labelling.
CON-TGO91-286 - Lundbeck Australia Pty Ltd

4 September 2020

Section 14, TGO91 consent

Product(s) approved for Supply with noncompliant labelling.
REXULTI brexpiprazole 2 mg film coated tablet blister pack (273223)

19 May 2017

ARTG

Australian Register of Therapeutic Goods (ARTG) information for REXULTI brexpiprazole 2 mg film coated tablet blister pack.
REXULTI brexpiprazole 3 mg film coated tablet blister pack (273221)

19 May 2017

ARTG

Australian Register of Therapeutic Goods (ARTG) information for REXULTI brexpiprazole 3 mg film coated tablet blister pack.
REXULTI brexpiprazole 4 mg film coated tablet blister pack (273224)

19 May 2017

ARTG

Australian Register of Therapeutic Goods (ARTG) information for REXULTI brexpiprazole 4 mg film coated tablet blister pack.
REXULTI brexpiprazole 1 mg film coated tablet blister pack (273220)

19 May 2017

ARTG

Australian Register of Therapeutic Goods (ARTG) information for REXULTI brexpiprazole 1 mg film coated tablet blister pack.
REXULTI brexpiprazole 0.5 mg film coated tablet blister pack (273222)

19 May 2017

ARTG

Australian Register of Therapeutic Goods (ARTG) information for REXULTI brexpiprazole 0.5 mg film coated tablet blister pack.
REXULTI brexpiprazole 0.25 mg film coated tablet blister pack (273225)

19 May 2017

ARTG

Australian Register of Therapeutic Goods (ARTG) information for REXULTI brexpiprazole 0.25 mg film coated tablet blister pack.
EBIXA memantine hydrochloride 10mg tablet blister pack Cancelled under Section 30(1)(c) of the Act

7 November 2019

Cancellation by sponsor

Requested by Lundbeck Australia Pty Ltd
SELINCRO nalmefene (as hydrochloride dihydrate) 18 mg film-coated tablet blister pack Cancelled under Section 30(1)(c) of the Act

7 November 2019

Cancellation by sponsor

Requested by Lundbeck Australia Pty Ltd

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