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Approvals
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TGA
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APOHEALTH RANITIDINE ACID & HEARTBURN RELIEF 150 mg (as hydrochloride) tablet blister pack
Approved
STANDARD
APOHEALTH RANITIDINE ACID & HEARTBURN RELIEF 150 mg (as hydrochloride) tablet blister pack
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
7d15d5458232e204
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
7d15d5458232e204
Product Name
APOHEALTH RANITIDINE ACID & HEARTBURN RELIEF 150 mg (as hydrochloride) tablet blister pack
Artg Id
254412
Artg Name
Suspended from ARTG - APOHEALTH RANITIDINE ACID & HEARTBURN RELIEF 150 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
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
7d15d5458232e204
Type
Standard
Back to TGA Approvals
APOHEALTH RANITIDINE ACID & HEARTBURN RELIEF 150 mg (as hydrochloride) tablet blister pack - TGA Drug Approval Details
