APO-ESCITALOPRAM escitalopram (as oxalate) 10 mg tablet blister

Arrotex Pharmaceuticals Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 8266847fd77d8116
Product Name: APO-ESCITALOPRAM escitalopram (as oxalate) 10 mg tablet blister
Artg Id: 213721
Artg Name: APO-ESCITALOPRAM escitalopram (as oxalate) 10 mg tablet blister
Sponsor: Arrotex Pharmaceuticals Pty Ltd
Company Detail Path: /organization/arrotex-pharmaceuticals-pty-ltd
Artg Date: 2013-11-06
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/6b054c5dae0685123ad608df16118c79.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/93930c8a4447ddc2cfdc5efcd85210a5.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

8266847fd77d8116

Type

Standard