Approvals/TGA/APO-VENLAFAXINE XR venlafaxine (as hydrochloride) 75 mg modified release capsule blister pack

Approved

STANDARD

APO-VENLAFAXINE XR venlafaxine (as hydrochloride) 75 mg modified release capsule blister pack

Arrotex Pharmaceuticals Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 48eea764a2d29501
Product Name: APO-VENLAFAXINE XR venlafaxine (as hydrochloride) 75 mg modified release capsule blister pack
Artg Id: 286958
Artg Name: APO-VENLAFAXINE XR venlafaxine (as hydrochloride) 75 mg modified release capsule blister pack
Sponsor: Arrotex Pharmaceuticals Pty Ltd
Company Detail Path: /organization/arrotex-pharmaceuticals-pty-ltd
Artg Date: 2017-06-23
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-2023-CMI-02015-1
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2023-PI-02014-1

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

48eea764a2d29501

Type

Standard