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

Approved

STANDARD

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

NOUMED PHARMACEUTICALS PTY LTD🇦🇺 Therapeutic Goods Administration

Approval Id: e22ffaa2abe031f9
Product Name: PRICELINE PHARMACY IBUPROFEN SODIUM Ibuprofen sodium dihydrate 256mg film coated tablet blister pack (new formulation)
Artg Id: 465348
Artg Name: PRICELINE PHARMACY 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

e22ffaa2abe031f9

Type

Standard