Approvals/TGA/NEBIVOLOL-WGR nebivolol (as hydrochloride) 1.25 mg tablet blister pack

Approved

STANDARD

NEBIVOLOL-WGR nebivolol (as hydrochloride) 1.25 mg tablet blister pack

GM Pharma International Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 9af5393fc70a828e
Product Name: NEBIVOLOL-WGR nebivolol (as hydrochloride) 1.25 mg tablet blister pack
Artg Id: 421915
Artg Name: NEBIVOLOL-WGR nebivolol (as hydrochloride) 1.25 mg tablet blister pack
Sponsor: GM Pharma International Pty Ltd
Company Detail Path: /organization/gm-pharma-international-pty-ltd
Artg Date: 2023-11-16
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/d7e07da0e8807e5f869b3fab8775ea10.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/dbf16015374febb0daca6a62f7b06f0a.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

9af5393fc70a828e

Type

Standard