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

Approved

STANDARD

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

Sandoz Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: e63e78b0fe499812
Product Name: DULOXETINE SANDOZ duloxetine (as hydrochloride) 30 mg enteric capsule blister pack
Artg Id: 199266
Artg Name: DULOXETINE SANDOZ duloxetine (as hydrochloride) 30 mg enteric capsule blister pack
Sponsor: Sandoz Pty Ltd
Company Detail Path: /organization/sandoz-pty-ltd
Artg Date: 2013-06-14
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2024-CMI-02955-1
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2024-PI-02954-1

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

e63e78b0fe499812

Type

Standard