NEBILET nebivolol (as hydrochloride) 10mg tablet blister pack

A Menarini Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 4d28ecf48585c8de
Product Name: NEBILET nebivolol (as hydrochloride) 10mg tablet blister pack
Artg Id: 148875
Artg Name: NEBILET nebivolol (as hydrochloride) 10mg tablet blister pack
Sponsor: A Menarini Australia Pty Ltd
Artg Date: 2009-06-26
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-02986-1
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2012-PI-02985-1

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

4d28ecf48585c8de

Type

Standard