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

Approved

STANDARD

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

Arrotex Pharmaceuticals Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 91f07024734bb9fa
Product Name: APO-NEBIVOLOL nebivolol (as hydrochloride) 1.25 mg tablet blister pack
Artg Id: 281799
Artg Name: APO-NEBIVOLOL nebivolol (as hydrochloride) 1.25 mg tablet blister pack
Sponsor: Arrotex Pharmaceuticals Pty Ltd
Company Detail Path: /organization/arrotex-pharmaceuticals-pty-ltd
Artg Date: 2018-02-21
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/fd0e5dc4c4d797a99228749e23f3dd14.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/bff4ff0501c401b01f4b043e409697ef.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

91f07024734bb9fa

Type

Standard