Approvals/TGA/DEPRETA 60 duloxetine 60 mg (as hydrochloride) enteric capsule bottle

Approved

STANDARD

DEPRETA 60 duloxetine 60 mg (as hydrochloride) enteric capsule bottle

Strides Pharma Science Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: e3f907586f195fc3
Product Name: DEPRETA 60 duloxetine 60 mg (as hydrochloride) enteric capsule bottle
Artg Id: 199002
Artg Name: DEPRETA 60 duloxetine 60 mg (as hydrochloride) enteric capsule bottle
Sponsor: Strides Pharma Science Pty Ltd
Company Detail Path: /organization/strides-pharma-science-pty-ltd
Artg Date: 2013-07-01
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-2013-CMI-01888-1
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2013-PI-01887-1

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

e3f907586f195fc3

Type

Standard