Approvals/TGA/CLEVIPREX clevidipine, 25 mg in 50 mL injectable emulsion, Single Use Vials

Approved

STANDARD

CLEVIPREX clevidipine, 25 mg in 50 mL injectable emulsion, Single Use Vials

Chiesi Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 2823ecbb8f091472
Product Name: CLEVIPREX clevidipine, 25 mg in 50 mL injectable emulsion, Single Use Vials
Artg Id: 203313
Artg Name: CLEVIPREX clevidipine, 25 mg in 50 mL injectable emulsion, Single Use Vials
Sponsor: Chiesi Australia Pty Ltd
Company Detail Path: /organization/chiesi-australia-pty-ltd
Artg Date: 2013-06-27
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-2021-CMI-01627-1
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2021-PI-01626-1

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

2823ecbb8f091472

Type

Standard