Approvals/TGA/BENDAMUSTINE SANDOZ bendamustine hydrochloride (as monohydrate) 25 mg powder for injection vial

Approved

STANDARD

BENDAMUSTINE SANDOZ bendamustine hydrochloride (as monohydrate) 25 mg powder for injection vial

Sandoz Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 9127f5b967f8402f
Product Name: BENDAMUSTINE SANDOZ bendamustine hydrochloride (as monohydrate) 25 mg powder for injection vial
Artg Id: 337201
Artg Name: BENDAMUSTINE SANDOZ bendamustine hydrochloride (as monohydrate) 25 mg powder for injection vial
Sponsor: Sandoz Pty Ltd
Company Detail Path: /organization/sandoz-pty-ltd
Artg Date: 2021-05-17
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-2023-CMI-01949-1
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2021-PI-01629-1

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

9127f5b967f8402f

Type

Standard