Approvals/TGA/XYNTHA moroctocog alfa (rch) 500IU powder for injection and diluent dual-chamber syringe

Approved

STANDARD

XYNTHA moroctocog alfa (rch) 500IU powder for injection and diluent dual-chamber syringe

Pfizer Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 8a900eb45429e883
Product Name: XYNTHA moroctocog alfa (rch) 500IU powder for injection and diluent dual-chamber syringe
Artg Id: 174838
Artg Name: XYNTHA moroctocog alfa (rch) 500IU 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: https://medical-cdn.nocode.com/drug_tga/dfd6e645418bf9dd6e45925db128fb92.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/5e092e63fda8db8fcfa93d9f4295f5b2.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

8a900eb45429e883

Type

Standard