Approvals/TGA/Venlafaxine XR-WGR venlafaxine (as hydrochloride) 225 mg modified release capsule

Approved

STANDARD

Venlafaxine XR-WGR venlafaxine (as hydrochloride) 225 mg modified release capsule

GM Pharma International Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 807f1301af22ad64
Product Name: Venlafaxine XR-WGR venlafaxine (as hydrochloride) 225 mg modified release capsule
Artg Id: 292623
Artg Name: Venlafaxine XR-WGR venlafaxine (as hydrochloride) 225 mg modified release capsule
Sponsor: GM Pharma International Pty Ltd
Company Detail Path: /organization/gm-pharma-international-pty-ltd
Artg Date: 2018-08-09
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Product Information: https://medical-cdn.nocode.com/drug_tga/bfca6cb9d588e438a4a5da537f21ccd3.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

807f1301af22ad64

Type

Standard