Approvals/TGA/NUROFEN DOUBLE STRENGTH ZAVANCE ibuprofen sodium dihydrate 512 mg sugar coated tablet blister pack

Approved

STANDARD

NUROFEN DOUBLE STRENGTH ZAVANCE ibuprofen sodium dihydrate 512 mg sugar coated tablet blister pack

Reckitt Benckiser Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 81a9e238df8939fe
Product Name: NUROFEN DOUBLE STRENGTH ZAVANCE ibuprofen sodium dihydrate 512 mg sugar coated tablet blister pack
Artg Id: 219883
Artg Name: NUROFEN DOUBLE STRENGTH ZAVANCE ibuprofen sodium dihydrate 512 mg sugar coated tablet blister pack
Sponsor: Reckitt Benckiser Pty Ltd
Company Detail Path: /organization/reckitt-benckiser-australia-pty-ltd
Artg Date: 2014-02-05
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

81a9e238df8939fe

Type

Standard