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ADIRAMEDICA NAPROXEN SODIUM 220 mg film coated tablet blister pack - TGA Drug Approval Details
Approvals
/
TGA
/
ADIRAMEDICA NAPROXEN SODIUM 220 mg film coated tablet blister pack
Approved
STANDARD
ADIRAMEDICA NAPROXEN SODIUM 220 mg film coated tablet blister pack
AdiraMedica Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
b2cf200b74827ca8
Company
AdiraMedica Pty Ltd
Type
Standard
Approval Details
Approval Id
b2cf200b74827ca8
Product Name
ADIRAMEDICA NAPROXEN SODIUM 220 mg film coated tablet blister pack
Artg Id
419010
Artg Name
ADIRAMEDICA NAPROXEN SODIUM 220 mg film coated tablet blister pack
Sponsor
AdiraMedica Pty Ltd
Company Detail Path
/organization/adiramedica-pty-ltd
Artg Date
2023-08-20
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
b2cf200b74827ca8
Type
Standard
Back to TGA Approvals
