Approvals/TGA/APO-CITALOPRAM citalopram 20 mg (as hydrobromide) tablet blister pack

Approved

STANDARD

APO-CITALOPRAM citalopram 20 mg (as hydrobromide) tablet blister pack

Arrotex Pharmaceuticals Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 9591e616941618f0
Product Name: APO-CITALOPRAM citalopram 20 mg (as hydrobromide) tablet blister pack
Artg Id: 226578
Artg Name: APO-CITALOPRAM citalopram 20 mg (as hydrobromide) tablet blister pack
Sponsor: Arrotex Pharmaceuticals Pty Ltd
Company Detail Path: /organization/arrotex-pharmaceuticals-pty-ltd
Artg Date: 2014-10-09
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/1ac4836b284e2df0afdba8ba658481d7.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/ddd69416d30a0dd53098ad9c7eac9933.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

9591e616941618f0

Type

Standard