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KYNTELES vedolizumab (rch) 300 mg powder for injection vial - TGA Drug Approval Details

Approvals/TGA/KYNTELES vedolizumab (rch) 300 mg powder for injection vial

Approved

STANDARD

KYNTELES vedolizumab (rch) 300 mg powder for injection vial

Takeda Pharmaceuticals Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Date: Dec 9, 2025
Approval ID: ae034cf18488efdc
Company: Takeda Pharmaceuticals Australia Pty Ltd
Type: Standard

Approval Details

Approval Id: ae034cf18488efdc
Product Name: KYNTELES vedolizumab (rch) 300 mg powder for injection vial
Artg Id: 210042
Artg Name: KYNTELES vedolizumab (rch) 300 mg powder for injection vial
Sponsor: Takeda Pharmaceuticals Australia Pty Ltd
Company Detail Path: /organization/takeda-pharmaceuticals-australia-pty-ltd
Artg Date: 2014-06-27
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE

Approved

Quick Info

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

ae034cf18488efdc

Type

Standard

Back to TGA Approvals