Approvals/TGA/NEBIVOLOL LUPIN nebivolol (as hydrochloride) 2.5 mg immediate release tablet blister pack

Approved

STANDARD

NEBIVOLOL LUPIN nebivolol (as hydrochloride) 2.5 mg immediate release tablet blister pack

Southern Cross Pharma Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 04a192b8e5c6dfc3
Product Name: NEBIVOLOL LUPIN nebivolol (as hydrochloride) 2.5 mg immediate release tablet blister pack
Artg Id: 311740
Artg Name: NEBIVOLOL LUPIN nebivolol (as hydrochloride) 2.5 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: https://medical-cdn.nocode.com/drug_tga/446c79f5ec70092ba9b42e4839909c40.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/fb863878e3a7de7a4e8aaf9c17b12a44.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

04a192b8e5c6dfc3

Type

Standard