Approvals/TGA/APOHEALTH RANITIDINE ACID & HEARTBURN RELIEF EXTRA STRENGTH 300 mg (as hydrochloride) tablet blister pack

Approved

STANDARD

APOHEALTH RANITIDINE ACID & HEARTBURN RELIEF EXTRA STRENGTH 300 mg (as hydrochloride) tablet blister pack

Arrotex Pharmaceuticals Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 8c924d0f71667cee
Product Name: APOHEALTH RANITIDINE ACID & HEARTBURN RELIEF EXTRA STRENGTH 300 mg (as hydrochloride) tablet blister pack
Artg Id: 254413
Artg Name: Suspended from ARTG - APOHEALTH RANITIDINE ACID & HEARTBURN RELIEF EXTRA STRENGTH 300 mg (as hydrochloride) tablet blister pack
Sponsor: Arrotex Pharmaceuticals Pty Ltd
Company Detail Path: /organization/arrotex-pharmaceuticals-pty-ltd
Artg Date: 2015-08-12
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

8c924d0f71667cee

Type

Standard