Approvals/TGA/BENEFIX factor IX recombinant 3000 IU powder for injection vial and diluent syringe composite pack

Approved

STANDARD

BENEFIX factor IX recombinant 3000 IU powder for injection vial and diluent syringe composite pack

Pfizer Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: c314b9525ff930c2
Product Name: BENEFIX factor IX recombinant 3000 IU powder for injection vial and diluent syringe composite pack
Artg Id: 203316
Artg Name: BENEFIX factor IX recombinant 3000 IU powder for injection vial and diluent syringe composite pack
Sponsor: Pfizer Australia Pty Ltd
Company Detail Path: /organization/pfizer-australia-pty-ltd
Artg Date: 2013-08-20
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/28ed7b175a23eb3bf56e005f043926a0.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/6a7637ed1adada34f922923c2f8238eb.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

c314b9525ff930c2

Type

Standard