Approvals/TGA/HEDAFEN IBUPROFEN 200 mg soft gelatin capsule blister pack (red capsules)

Approved

STANDARD

HEDAFEN IBUPROFEN 200 mg soft gelatin capsule blister pack (red capsules)

Nova Pharmaceuticals Australasia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: b30123b9a552c36f
Product Name: HEDAFEN IBUPROFEN 200 mg soft gelatin capsule blister pack (red capsules)
Artg Id: 210582
Artg Name: HEDAFEN IBUPROFEN 200 mg soft gelatin capsule blister pack (red capsules)
Sponsor: Nova Pharmaceuticals Australasia Pty Ltd
Company Detail Path: /organization/nova-pharmaceuticals-australasia-pty-ltd
Artg Date: 2013-06-05
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

b30123b9a552c36f

Type

Standard