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HEDAFEN IBUPROFEN 200 mg sugar-coated tablet blister pack - TGA Drug Approval Details
Approvals
/
TGA
/
HEDAFEN IBUPROFEN 200 mg sugar-coated tablet blister pack
Approved
STANDARD
HEDAFEN IBUPROFEN 200 mg sugar-coated tablet blister pack
Nova Pharmaceuticals Australasia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 29, 2025
Approval ID
3d6ce44004e38b49
Company
Nova Pharmaceuticals Australasia Pty Ltd
Type
Standard
Approval Details
Approval Id
3d6ce44004e38b49
Product Name
HEDAFEN IBUPROFEN 200 mg sugar-coated tablet blister pack
Artg Id
202495
Artg Name
HEDAFEN IBUPROFEN 200 mg sugar-coated tablet blister pack
Sponsor
Nova Pharmaceuticals Australasia Pty Ltd
Company Detail Path
/organization/nova-pharmaceuticals-australasia-pty-ltd
Artg Date
2012-10-29
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 29, 2025
Approval ID
3d6ce44004e38b49
Type
Standard
Back to TGA Approvals
