Approvals/TGA/SOLU-CORTEF ACT-O-VIAL 500mg powder for injection and diluent in one vial

Approved

STANDARD

SOLU-CORTEF ACT-O-VIAL 500mg powder for injection and diluent in one vial

Pfizer Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: a002387af3739722
Product Name: SOLU-CORTEF ACT-O-VIAL 500mg powder for injection and diluent in one vial
Artg Id: 167895
Artg Name: SOLU-CORTEF ACT-O-VIAL hydrocortisone (as sodium succinate) 500mg powder for injection and diluent in one vial
Sponsor: Pfizer Australia Pty Ltd
Company Detail Path: /organization/pfizer-australia-pty-ltd
Artg Date: 2010-03-05
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-05479-3
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2010-PI-05478-3

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

a002387af3739722

Type

Standard