Approvals/TGA/CITALOPRAM AMNEAL citalopram (as hydrobromide) 10 mg tablet blister pack

Approved

STANDARD

CITALOPRAM AMNEAL citalopram (as hydrobromide) 10 mg tablet blister pack

Arrotex Pharmaceuticals Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: feb7407935061525
Product Name: CITALOPRAM AMNEAL citalopram (as hydrobromide) 10 mg tablet blister pack
Artg Id: 158879
Artg Name: CITALOPRAM AMNEAL citalopram (as hydrobromide) 10 mg tablet blister pack
Sponsor: Arrotex Pharmaceuticals Pty Ltd
Company Detail Path: /organization/arrotex-pharmaceuticals-pty-ltd
Artg Date: 2010-02-12
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/a4c7460e88694073befbb062bec6e218.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/affa372769811b3eca9d269048298e71.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

feb7407935061525

Type

Standard