Approvals/TGA/CEFTRIAXONE-AFT ceftriaxone (as sodium) 500 mg powder for injection vial

Approved

STANDARD

CEFTRIAXONE-AFT ceftriaxone (as sodium) 500 mg powder for injection vial

AFT Pharmaceuticals Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 37a65487841b8c1e
Product Name: CEFTRIAXONE-AFT ceftriaxone (as sodium) 500 mg powder for injection vial
Artg Id: 185099
Artg Name: CEFTRIAXONE-AFT ceftriaxone (as sodium) 500 mg powder for injection vial
Sponsor: AFT Pharmaceuticals Pty Ltd
Company Detail Path: /organization/aft-pharmaceuticals-au-pty-ltd
Artg Date: 2012-02-20
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-2012-CMI-01381-3
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2012-PI-01380-3

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

37a65487841b8c1e

Type

Standard