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

Approved

STANDARD

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

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

Approval Id: ffe0f9475cc55bd9
Product Name: PRICELINE IBUPROFEN SODIUM 256mg (as sodium dihydrate) film coated tablet blister pack (new formulation)
Artg Id: 408196
Artg Name: PRICELINE IBUPROFEN SODIUM 256mg (as sodium dihydrate) film coated tablet blister pack (new formulation)
Sponsor: Neo Health (OTC) Pty Ltd
Company Detail Path: /organization/neo-health-otc-pty-ltd
Artg Date: 2023-04-27
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

ffe0f9475cc55bd9

Type

Standard