Approvals/TGA/ADYNOVATE rurioctocog alfa pegol (rch) 3000 IU powder for injection vial with diluent vial

Approved

STANDARD

ADYNOVATE rurioctocog alfa pegol (rch) 3000 IU powder for injection vial with diluent vial

Takeda Pharmaceuticals Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: f2dcd46e44a680cc
Product Name: ADYNOVATE rurioctocog alfa pegol (rch) 3000 IU powder for injection vial with diluent vial
Artg Id: 300852
Artg Name: ADYNOVATE rurioctocog alfa pegol (rch) 3000 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: 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

f2dcd46e44a680cc

Type

Standard