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MEDIX IBUPROFEN 200 mg soft gelatin capsule blister pack - TGA Drug Approval Details
Approvals
/
TGA
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MEDIX IBUPROFEN 200 mg soft gelatin capsule blister pack
Approved
STANDARD
MEDIX IBUPROFEN 200 mg soft gelatin capsule blister pack
Nova Pharmaceuticals Australasia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
6a3fd3f2c5edb341
Company
Nova Pharmaceuticals Australasia Pty Ltd
Type
Standard
Approval Details
Approval Id
6a3fd3f2c5edb341
Product Name
MEDIX IBUPROFEN 200 mg soft gelatin capsule blister pack
Artg Id
165905
Artg Name
MEDIX IBUPROFEN 200 mg soft gelatin capsule blister pack
Sponsor
Nova Pharmaceuticals Australasia Pty Ltd
Company Detail Path
/organization/nova-pharmaceuticals-australasia-pty-ltd
Artg Date
2009-10-07
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
6a3fd3f2c5edb341
Type
Standard
Back to TGA Approvals
