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

Approved

STANDARD

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

NOUMED PHARMACEUTICALS PTY LTD🇦🇺 Therapeutic Goods Administration

Approval Id: c67f4e225bd409d1
Product Name: PHARMACY CHOICE IBUPROFEN SODIUM Ibuprofen sodium dihydrate 256mg film coated tablet blister pack (new formulation)
Artg Id: 465328
Artg Name: PHARMACY CHOICE IBUPROFEN SODIUM Ibuprofen sodium dihydrate 256mg film coated tablet blister pack (new formulation)
Sponsor: NOUMED PHARMACEUTICALS PTY LTD
Company Detail Path: /organization/noumed-pharmaceuticals-pty-ltd
Artg Date: 2024-10-22
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

c67f4e225bd409d1

Type

Standard