Approvals/TGA/ADYNOVATE rurioctocog alfa pegol (rch) 500 IU powder for injection vial with diluent vial

Approved

STANDARD

ADYNOVATE rurioctocog alfa pegol (rch) 500 IU powder for injection vial with diluent vial

Takeda Pharmaceuticals Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: e5b4af67061929c7
Product Name: ADYNOVATE rurioctocog alfa pegol (rch) 500 IU powder for injection vial with diluent vial
Artg Id: 278727
Artg Name: ADYNOVATE rurioctocog alfa pegol (rch) 500 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: 2017-03-21
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/81f9020fcd6e70fd03c8a0beff997807.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/f3e6f1bbbfb379db46c71bd792a90ca7.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

e5b4af67061929c7

Type

Standard