Approvals/TGA/BENEFIX factor IX recombinant 2000 IU powder for injection vial and diluent syringe composite pack

Approved

STANDARD

BENEFIX factor IX recombinant 2000 IU powder for injection vial and diluent syringe composite pack

Pfizer Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 8187f9b6b146bc69
Product Name: BENEFIX factor IX recombinant 2000 IU powder for injection vial and diluent syringe composite pack
Artg Id: 128378
Artg Name: BENEFIX factor IX recombinant 2000 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: 2007-09-27
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2010-CMI-05099-3
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2010-PI-05100-3

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

8187f9b6b146bc69

Type

Standard