GLAUMOX acetazolamide (as sodium) 500 mg powder for injection vial

Phebra Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 71680a361627b367
Product Name: GLAUMOX acetazolamide (as sodium) 500 mg powder for injection vial
Artg Id: 142075
Artg Name: GLAUMOX acetazolamide (as sodium) 500 mg powder for injection vial
Sponsor: Phebra Pty Ltd
Company Detail Path: /organization/phebra-pty-ltd
Artg Date: 2009-06-01
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-2010-CMI-02584-3
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2010-PI-02583-3

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

71680a361627b367

Type

Standard