Approvals/TGA/APO-ATOMOXETINE atomoxetine (as hydrochloride) 18 mg capsule blister

Approved

STANDARD

APO-ATOMOXETINE atomoxetine (as hydrochloride) 18 mg capsule blister

Arrotex Pharmaceuticals Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 2548826338849fb6
Product Name: APO-ATOMOXETINE atomoxetine (as hydrochloride) 18 mg capsule blister
Artg Id: 290980
Artg Name: APO-ATOMOXETINE atomoxetine (as hydrochloride) 18 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

2548826338849fb6

Type

Standard