Approvals/TGA/CITALOPRAM SANDOZ citalopram 20mg (as hydrobromide) film coated tablet blister pack

Approved

STANDARD

CITALOPRAM SANDOZ citalopram 20mg (as hydrobromide) film coated tablet blister pack

Sandoz Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: caee10dd19c5972c
Product Name: CITALOPRAM SANDOZ citalopram 20mg (as hydrobromide) film coated tablet blister pack
Artg Id: 101691
Artg Name: CITALOPRAM SANDOZ citalopram 20mg (as hydrobromide) film coated tablet blister pack
Sponsor: Sandoz Pty Ltd
Company Detail Path: /organization/sandoz-pty-ltd
Artg Date: 2004-06-08
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-2015-CMI-02608-1
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2023-PI-01860-1

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

caee10dd19c5972c

Type

Standard