Approvals/TGA/Venlafaxine XR-WGR venlafaxine (as hydrochloride) 37.5 mg modified release capsule blister pack

Approved

STANDARD

Venlafaxine XR-WGR venlafaxine (as hydrochloride) 37.5 mg modified release capsule blister pack

GM Pharma International Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 0c913c3eeb10cc73
Product Name: Venlafaxine XR-WGR venlafaxine (as hydrochloride) 37.5 mg modified release capsule blister pack
Artg Id: 285257
Artg Name: Venlafaxine XR-WGR venlafaxine (as hydrochloride) 37.5 mg modified release capsule blister pack
Sponsor: GM Pharma International Pty Ltd
Company Detail Path: /organization/gm-pharma-international-pty-ltd
Artg Date: 2017-05-17
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2024-CMI-02843-1
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2024-PI-01730-1

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

0c913c3eeb10cc73

Type

Standard