NEBILET nebivolol (as hydrochloride) 1.25mg tablet blister pack

A Menarini Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: b1086eab24dfcbfc
Product Name: NEBILET nebivolol (as hydrochloride) 1.25mg tablet blister pack
Artg Id: 148873
Artg Name: NEBILET nebivolol (as hydrochloride) 1.25mg 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

Dec 9, 2025

Approval ID

b1086eab24dfcbfc

Type

Standard