Approvals/TGA/FLUOXETINE SANDOZ fluoxetine (as hydrochloride) 20mg capsule blister pack

Approved

STANDARD

FLUOXETINE SANDOZ fluoxetine (as hydrochloride) 20mg capsule blister pack

Sandoz Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 25d64afc9c7a20e6
Product Name: FLUOXETINE SANDOZ fluoxetine (as hydrochloride) 20mg capsule blister pack
Artg Id: 64564
Artg Name: FLUOXETINE SANDOZ fluoxetine (as hydrochloride) 20mg capsule blister pack
Sponsor: Sandoz Pty Ltd
Company Detail Path: /organization/sandoz-pty-ltd
Artg Date: 1998-06-09
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-2012-CMI-01167-3
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2011-PI-03135-3

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

25d64afc9c7a20e6

Type

Standard