Approvals/TGA/Venlafaxine XR-WGR venlafaxine (as hydrochloride) 150 mg modified release capsule blister pack

Approved

STANDARD

Venlafaxine XR-WGR venlafaxine (as hydrochloride) 150 mg modified release capsule blister pack

GM Pharma International Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 44f604c932ddde08
Product Name: Venlafaxine XR-WGR venlafaxine (as hydrochloride) 150 mg modified release capsule blister pack
Artg Id: 285259
Artg Name: Venlafaxine XR-WGR venlafaxine (as hydrochloride) 150 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: https://medical-cdn.nocode.com/drug_tga/9335956e877e3517740e2eba089fcf60.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/bfca6cb9d588e438a4a5da537f21ccd3.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

44f604c932ddde08

Type

Standard