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

Approved

STANDARD

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

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

Approval Id: dd0117405235dc2d
Product Name: PHARMACY HEALTH IBUPROFEN SODIUM 256mg (as sodium dihydrate) film coated tablet blister pack (new formulation)
Artg Id: 408195
Artg Name: PHARMACY HEALTH 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

dd0117405235dc2d

Type

Standard