Approvals/TGA/MONOFIX-VF human coagulation factor IX 500IU powder for injection vial and diluent vial

Approved

STANDARD

MONOFIX-VF human coagulation factor IX 500IU powder for injection vial and diluent vial

CSL Behring (Australia) Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: f402cf4eec2936dd
Product Name: MONOFIX-VF human coagulation factor IX 500IU powder for injection vial and diluent vial
Artg Id: 66066
Artg Name: MONOFIX-VF human coagulation factor IX 500IU powder for injection vial and diluent vial
Sponsor: CSL Behring (Australia) Pty Ltd
Company Detail Path: /organization/csl-behring-australia-pty-ltd
Artg Date: 1998-11-24
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/a2c317fd515e375ea6f086b020cfe354.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/c8114dcbdfaa8f6beef60eb374c6b624.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

f402cf4eec2936dd

Type

Standard