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PRICELINE IBUPROFEN SODIUM ibuprofen sodium dihydrate 256mg tablet blister pack - TGA Drug Approval Details
Approvals
/
TGA
/
PRICELINE IBUPROFEN SODIUM ibuprofen sodium dihydrate 256mg tablet blister pack
Approved
STANDARD
PRICELINE IBUPROFEN SODIUM ibuprofen sodium dihydrate 256mg tablet blister pack
AdiraMedica Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
f1336a6669e86710
Company
AdiraMedica Pty Ltd
Type
Standard
Approval Details
Approval Id
f1336a6669e86710
Product Name
PRICELINE IBUPROFEN SODIUM ibuprofen sodium dihydrate 256mg tablet blister pack
Artg Id
315545
Artg Name
PRICELINE IBUPROFEN SODIUM ibuprofen sodium dihydrate 256mg tablet blister pack
Sponsor
AdiraMedica Pty Ltd
Company Detail Path
/organization/adiramedica-pty-ltd
Artg Date
2019-03-19
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
f1336a6669e86710
Type
Standard
Back to TGA Approvals
