Escitalopram Tablet, Film Coated
Product Images NDC 71205-193

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Escitalopram (NDC 71205-193). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

71205-193-30 (Escitalopram Fig5)

Escitalopram 20 mg tablet label from Proficient Rx LP. The label indicates 30 film-coated tablets per package for oral use. It includes storage instructions, manufacturer information (Aurobindo Pharma Limited, India), and product ID QE019330. The label highlights that each tablet contains escitalopram oxalate equivalent to 20 mg escitalopram base and displays regulatory details such as NDC 71205-193-30 and RX only status.*

FDA Label Image

Chemical Structure (Escitalopram Str)

Chemical structure of Escitalopram Oxalate, showing the molecular arrangement including a fluorophenyl group, a nitrile-substituted phenyl ring, and the oxalate moiety. The structure clearly depicts atoms and bonds relevant to the active ingredient Escitalopram Oxalate.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.