APO-MEBEVERINE mebeverine hydrochloride 135 mg tablet blister pack

Arrotex Pharmaceuticals Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 9739bf8eb3acad46
Product Name: APO-MEBEVERINE mebeverine hydrochloride 135 mg tablet blister pack
Artg Id: 288817
Artg Name: APO-MEBEVERINE mebeverine hydrochloride 135 mg tablet blister pack
Sponsor: Arrotex Pharmaceuticals Pty Ltd
Company Detail Path: /organization/arrotex-pharmaceuticals-pty-ltd
Artg Date: 2018-04-04
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/73ef5bbbbc0e1666cb6664e1c86a5588.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/76ed4391443c8e5db5d3dd67a118bbde.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

9739bf8eb3acad46

Type

Standard