Approvals/TGA/NEBIVOLOL SANDOZ nebivolol (as hydrochloride) 5 mg immediate release tablet blister pack

Approved

STANDARD

NEBIVOLOL SANDOZ nebivolol (as hydrochloride) 5 mg immediate release tablet blister pack

Southern Cross Pharma Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 13901f0f489ceafe
Product Name: NEBIVOLOL SANDOZ nebivolol (as hydrochloride) 5 mg immediate release tablet blister pack
Artg Id: 311724
Artg Name: NEBIVOLOL SANDOZ nebivolol (as hydrochloride) 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/26a6306c864737b9c8545810934012a0.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/d15bb4167d7715c9e1e266848e77d8d3.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

13901f0f489ceafe

Type

Standard