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Teva Pharma Australia Pty Ltd

Regulatory activities for this sponsor.

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Type

Cancellation by sponsor (174)
ARTG (106)
Prescription medicine registration (26)
Australian public assessment report (AusPar) (7)
Prescription medicine decision summary (3)
Section 14, TGO91 consent (2)
Designation or determination (1)
Prescription medicine evaluation (1)

Date

2026 (4)
2025 (32)
2024 (120)
2023 (16)
2022 (13)
2021 (61)
2020 (23)
2019 (9)
2018 (5)
2017 (7)
2016 (18)
2015 (2)
2012 (1)
2011 (4)
2006 (3)
1995 (2)

Search

Sponsor content

320 result(s) found, displaying 31 to 40

BI-EASE DUO ALLERGY azelastine (as hydrochloride) 125 microgram and fluticasone propionate 50 microgram nasal spray bottle (415711)

25 September 2024

ARTG

Australian Register of Therapeutic Goods (ARTG) information for BI-EASE DUO ALLERGY azelastine (as hydrochloride) 125 microgram and fluticasone propionate 50 microgram nasal spray bottle.
LENALIDOMIDE-TEVA lenalidomide (as hydrochloride monohydrate) 10 mg capsule blister pack Cancelled under Section 30(1)(c) of the Act

7 March 2025

Cancellation by sponsor

Requested by Teva Pharma Australia Pty Ltd
LENALIDOMIDE-TEVA lenalidomide (as hydrochloride monohydrate) 25 mg capsule blister pack Cancelled under Section 30(1)(c) of the Act

7 March 2025

Cancellation by sponsor

Requested by Teva Pharma Australia Pty Ltd
LENALIDOMIDE-TEVA lenalidomide (as hydrochloride monohydrate) 15 mg capsule blister pack Cancelled under Section 30(1)(c) of the Act

7 March 2025

Cancellation by sponsor

Requested by Teva Pharma Australia Pty Ltd
LENALIDOMIDE-TEVA lenalidomide (as hydrochloride monohydrate) 7.5 mg capsule blister pack Cancelled under Section 30(1)(c) of the Act

7 March 2025

Cancellation by sponsor

Requested by Teva Pharma Australia Pty Ltd
LENALIDOMIDE-TEVA lenalidomide (as hydrochloride monohydrate) 20 mg capsule blister pack Cancelled under Section 30(1)(c) of the Act

7 March 2025

Cancellation by sponsor

Requested by Teva Pharma Australia Pty Ltd
LENALIDOMIDE-TEVA lenalidomide (as hydrochloride monohydrate) 5 mg capsule blister pack Cancelled under Section 30(1)(c) of the Act

7 March 2025

Cancellation by sponsor

Requested by Teva Pharma Australia Pty Ltd
LENALIDOMIDE-TEVA lenalidomide (as hydrochloride monohydrate) 2.5 mg capsule blister pack Cancelled under Section 30(1)(c) of the Act

7 March 2025

Cancellation by sponsor

Requested by Teva Pharma Australia Pty Ltd
PALIPERIDONE-TEVA paliperidone (as palmitate) 75 mg/0.75 mL modified release suspension for injection pre-filled syringe (404390)

5 June 2024

ARTG

Australian Register of Therapeutic Goods (ARTG) information for PALIPERIDONE-TEVA paliperidone (as palmitate) 75 mg/0.75 mL modified release suspension for injection pre-filled syringe.
PALIPERIDONE-TEVA paliperidone (as palmitate) 100 mg/1.0 mL modified release suspension for injection pre-filled syringe (404391)

5 June 2024

ARTG

Australian Register of Therapeutic Goods (ARTG) information for PALIPERIDONE-TEVA paliperidone (as palmitate) 100 mg/1.0 mL modified release suspension for injection pre-filled syringe.

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