Approvals/TGA/ALENDRO ONCE-WEEKLY alendronic acid 70 mg (as sodium alendronate monohydrate) tablet blister pack

Approved

STANDARD

ALENDRO ONCE-WEEKLY alendronic acid 70 mg (as sodium alendronate monohydrate) tablet blister pack

Arrotex Pharmaceuticals Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 97d5d69c18956866
Product Name: ALENDRO ONCE-WEEKLY alendronic acid 70 mg (as sodium alendronate monohydrate) tablet blister pack
Artg Id: 100691
Artg Name: ALENDRO ONCE-WEEKLY alendronic acid 70 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 30, 2025

Approval ID

97d5d69c18956866

Type

Standard