Approvals/TGA/TERRYWHITE CHEMMART IBUPROFEN SODIUM Ibuprofen sodium dihydrate 256mg film coated tablet blister pack (new formulation)

Approved

STANDARD

TERRYWHITE CHEMMART IBUPROFEN SODIUM Ibuprofen sodium dihydrate 256mg film coated tablet blister pack (new formulation)

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

Approval Id: a5758072e0e6d68f
Product Name: TERRYWHITE CHEMMART IBUPROFEN SODIUM Ibuprofen sodium dihydrate 256mg film coated tablet blister pack (new formulation)
Artg Id: 402305
Artg Name: TERRYWHITE CHEMMART IBUPROFEN SODIUM Ibuprofen sodium dihydrate 256mg film coated tablet blister pack (new formulation)
Sponsor: Neo Health (OTC) Pty Ltd
Company Detail Path: /organization/neo-health-otc-pty-ltd
Artg Date: 2023-01-17
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

a5758072e0e6d68f

Type

Standard