Approvals/TGA/ATOMOXETINE SANDOZ atomoxetine (as hydrochloride) 18 mg capsule blister pack

Approved

STANDARD

ATOMOXETINE SANDOZ atomoxetine (as hydrochloride) 18 mg capsule blister pack

Sandoz Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: bdf7670e4a3d6311
Product Name: ATOMOXETINE SANDOZ atomoxetine (as hydrochloride) 18 mg capsule blister pack
Artg Id: 238367
Artg Name: ATOMOXETINE SANDOZ atomoxetine (as hydrochloride) 18 mg capsule blister pack
Sponsor: Sandoz Pty Ltd
Company Detail Path: /organization/sandoz-pty-ltd
Artg Date: 2015-11-10
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/932ff4451e25aef4eca183ed8862b801.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/06b95053e1d58db3c3ffe63349ebc966.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

bdf7670e4a3d6311

Type

Standard