Approvals/TGA/APO-DULOXETINE duloxetine (as hydrochloride) 30 mg enteric capsule blister pack

Approved

STANDARD

APO-DULOXETINE duloxetine (as hydrochloride) 30 mg enteric capsule blister pack

Arrotex Pharmaceuticals Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: f71db499fb85ef2e
Product Name: APO-DULOXETINE duloxetine (as hydrochloride) 30 mg enteric capsule blister pack
Artg Id: 427036
Artg Name: APO-DULOXETINE duloxetine (as hydrochloride) 30 mg enteric capsule blister pack
Sponsor: Arrotex Pharmaceuticals Pty Ltd
Company Detail Path: /organization/arrotex-pharmaceuticals-pty-ltd
Artg Date: 2024-09-20
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/fb762eb24cc9af8eee316bda31446a69.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/e83fd6748c3770f71e1f2d1197eef865.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

f71db499fb85ef2e

Type

Standard