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

Approved

STANDARD

APO-VENLAFAXINE XR venlafaxine (as hydrochloride) 150 mg modified release capsule blister pack

Arrotex Pharmaceuticals Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: bbd0607ca778527d
Product Name: APO-VENLAFAXINE XR venlafaxine (as hydrochloride) 150 mg modified release capsule blister pack
Artg Id: 286957
Artg Name: APO-VENLAFAXINE XR venlafaxine (as hydrochloride) 150 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: https://medical-cdn.nocode.com/drug_tga/a7b9be6a36df198f728a9a4ca7ae1669.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/95c1ed0106ea2f4855127c6840e728b1.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

bbd0607ca778527d

Type

Standard