Approvals/TGA/ALENDRO 10 alendronic acid 10 mg (as sodium alendronate monohydrate) tablet blister pack

Approved

STANDARD

ALENDRO 10 alendronic acid 10 mg (as sodium alendronate monohydrate) tablet blister pack

Arrotex Pharmaceuticals Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 0ef5a3bb190c8e1f
Product Name: ALENDRO 10 alendronic acid 10 mg (as sodium alendronate monohydrate) tablet blister pack
Artg Id: 100688
Artg Name: ALENDRO 10 alendronic acid 10 mg (as sodium alendronate monohydrate) tablet blister pack
Sponsor: Arrotex Pharmaceuticals Pty Ltd
Company Detail Path: /organization/arrotex-pharmaceuticals-pty-ltd
Artg Date: 2005-05-27
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 29, 2025

Approval ID

0ef5a3bb190c8e1f

Type

Standard