Approvals/TGA/XYNTHA moroctocog alfa (rch) 3000IU powder for injection and diluent dual-chamber syringe

Approved

STANDARD

XYNTHA moroctocog alfa (rch) 3000IU powder for injection and diluent dual-chamber syringe

Pfizer Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 7ab5bc4f30ee4329
Product Name: XYNTHA moroctocog alfa (rch) 3000IU powder for injection and diluent dual-chamber syringe
Artg Id: 174841
Artg Name: XYNTHA moroctocog alfa (rch) 3000IU powder for injection and diluent dual-chamber syringe
Sponsor: Pfizer Australia Pty Ltd
Company Detail Path: /organization/pfizer-australia-pty-ltd
Artg Date: 2011-10-04
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-06727-3
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2010-PI-06728-3

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

7ab5bc4f30ee4329

Type

Standard