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

Approved

STANDARD

NEBIVOLOL VIATRIS nebivolol (as hydrochloride) 1.25 mg tablet blister pack

Helix Pharmaceuticals Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 60f5e0bf9d92fe67
Product Name: NEBIVOLOL VIATRIS nebivolol (as hydrochloride) 1.25 mg tablet blister pack
Artg Id: 281797
Artg Name: NEBIVOLOL VIATRIS nebivolol (as hydrochloride) 1.25 mg tablet blister pack
Sponsor: Helix Pharmaceuticals Pty Ltd
Company Detail Path: /organization/helix-pharmaceuticals-pty-ltd
Artg Date: 2018-02-21
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

60f5e0bf9d92fe67

Type

Standard