Approvals/TGA/APO-DULOXETINE duloxetine (as hydrochloride) 60 mg enteric capsule blister pack

Approved

STANDARD

APO-DULOXETINE duloxetine (as hydrochloride) 60 mg enteric capsule blister pack

Arrotex Pharmaceuticals Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 14ba83cd1ee96192
Product Name: APO-DULOXETINE duloxetine (as hydrochloride) 60 mg enteric capsule blister pack
Artg Id: 217986
Artg Name: APO-DULOXETINE duloxetine (as hydrochloride) 60 mg enteric capsule blister pack
Sponsor: Arrotex Pharmaceuticals Pty Ltd
Company Detail Path: /organization/arrotex-pharmaceuticals-pty-ltd
Artg Date: 2014-02-20
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/4ab6ad030b2e7000112875cadc089056.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/58a685cb40af9cd8c29c3d62ac771b78.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

14ba83cd1ee96192

Type

Standard