Approvals/TGA/ADYNOVATE rurioctocog alfa pegol (rch) 750 IU powder for injection vial with diluent vial

Approved

STANDARD

ADYNOVATE rurioctocog alfa pegol (rch) 750 IU powder for injection vial with diluent vial

Takeda Pharmaceuticals Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 72be04e5998fed1f
Product Name: ADYNOVATE rurioctocog alfa pegol (rch) 750 IU powder for injection vial with diluent vial
Artg Id: 300850
Artg Name: ADYNOVATE rurioctocog alfa pegol (rch) 750 IU powder for injection vial with diluent vial
Sponsor: Takeda Pharmaceuticals Australia Pty Ltd
Company Detail Path: /organization/takeda-pharmaceuticals-australia-pty-ltd
Artg Date: 2019-01-29
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-2017-CMI-01494-1
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2017-PI-01493-1

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

72be04e5998fed1f

Type

Standard