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ADIRAMEDICA IBUPROFEN SODIUM ibuprofen sodium dihydrate 256mg film coated tablet blister pack - TGA Drug Approval Details
Approvals
/
TGA
/
ADIRAMEDICA IBUPROFEN SODIUM ibuprofen sodium dihydrate 256mg film coated tablet blister pack
Approved
STANDARD
ADIRAMEDICA IBUPROFEN SODIUM ibuprofen sodium dihydrate 256mg film coated tablet blister pack
AdiraMedica Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
c47b6dd20fe2ad5e
Company
AdiraMedica Pty Ltd
Type
Standard
Approval Details
Approval Id
c47b6dd20fe2ad5e
Product Name
ADIRAMEDICA IBUPROFEN SODIUM ibuprofen sodium dihydrate 256mg film coated tablet blister pack
Artg Id
315542
Artg Name
ADIRAMEDICA IBUPROFEN SODIUM ibuprofen sodium dihydrate 256mg film coated 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
c47b6dd20fe2ad5e
Type
Standard
Back to TGA Approvals
