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NALTREXONE-APOTEX naltrexone hydrochloride 50 mg film coated tablets bottle - TGA Drug Approval Details
Approvals
/
TGA
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NALTREXONE-APOTEX naltrexone hydrochloride 50 mg film coated tablets bottle
Approved
STANDARD
NALTREXONE-APOTEX naltrexone hydrochloride 50 mg film coated tablets bottle
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
1f6f138785e816c7
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
1f6f138785e816c7
Product Name
NALTREXONE-APOTEX naltrexone hydrochloride 50 mg film coated tablets bottle
Artg Id
271012
Artg Name
NALTREXONE-APOTEX naltrexone hydrochloride 50 mg film coated tablets bottle
Sponsor
Arrotex Pharmaceuticals Pty Ltd
Company Detail Path
/organization/arrotex-pharmaceuticals-pty-ltd
Artg Date
2017-01-24
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
1f6f138785e816c7
Type
Standard
Back to TGA Approvals
