Approvals/TGA/AMCAL+ IBUPROFEN SODIUM DIHYDRATE 256 MG film coated tablet blister pack

Approved

STANDARD

AMCAL+ IBUPROFEN SODIUM DIHYDRATE 256 MG film coated tablet blister pack

Neo Health (OTC) Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: cc9dc28add1cfcc9
Product Name: AMCAL+ IBUPROFEN SODIUM DIHYDRATE 256 MG film coated tablet blister pack
Artg Id: 443150
Artg Name: AMCAL+ IBUPROFEN SODIUM DIHYDRATE 256 MG film coated tablet blister pack
Sponsor: Neo Health (OTC) Pty Ltd
Company Detail Path: /organization/neo-health-otc-pty-ltd
Artg Date: 2024-03-04
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

cc9dc28add1cfcc9

Type

Standard