Approvals/TGA/APO-ATOMOXETINE atomoxetine (as hydrochloride) 25 mg capsule blister

Approved

STANDARD

APO-ATOMOXETINE atomoxetine (as hydrochloride) 25 mg capsule blister

Arrotex Pharmaceuticals Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 95e04f067b878db5
Product Name: APO-ATOMOXETINE atomoxetine (as hydrochloride) 25 mg capsule blister
Artg Id: 290981
Artg Name: APO-ATOMOXETINE atomoxetine (as hydrochloride) 25 mg capsule blister
Sponsor: Arrotex Pharmaceuticals Pty Ltd
Company Detail Path: /organization/arrotex-pharmaceuticals-pty-ltd
Artg Date: 2017-09-29
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/c3a3758625645f7b14cd6eb1bf381986.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/f9192ad0a2ba36970f8978784020dc8e.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

95e04f067b878db5

Type

Standard