Approvals/TGA/NEBIVOLOL LUPIN nebivolol (as hydrochloride)1.25 mg immediate release tablet blister pack

Approved

STANDARD

NEBIVOLOL LUPIN nebivolol (as hydrochloride)1.25 mg immediate release tablet blister pack

Southern Cross Pharma Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 2bcf29bc248f641c
Product Name: NEBIVOLOL LUPIN nebivolol (as hydrochloride)1.25 mg immediate release tablet blister pack
Artg Id: 311739
Artg Name: NEBIVOLOL LUPIN nebivolol (as hydrochloride)1.25 mg immediate release tablet blister pack
Sponsor: Southern Cross Pharma Pty Ltd
Company Detail Path: /organization/southern-cross-pharma-pty-ltd
Artg Date: 2020-04-03
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-01590-1
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2020-PI-01408-1

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

2bcf29bc248f641c

Type

Standard