Escitalopram Oxalate
Product Images NDC 61919-139

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Escitalopram Oxalate (NDC 61919-139). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct Rx, 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

Image Description (Escitalopram10,60)

Image Description (Escitalopram10,60)
ESCITALOPRAM OXALATE 10 mg film-coated tablets, 60 count bottle label. The label identifies the product as a generic for Lexapro, containing escitalopram oxalate equivalent to 10 mg escitalopram. It is distributed by Direct Rx in Alpharetta, GA, with product number 139-60 and discard date 01/17 shown. Instructions and warnings such as "Keep out of reach of children" and patient information details are partially visible.*
FDA Label Image

Image Description (Label)

Image Description (Label)
ESCITALOPRAM 10mg 30 Tablets carton label for the generic drug Lexapro. The label states each film-coated tablet contains escitalopram oxalate equivalent to 10 mg escitalopram. Packaged and distributed by Direct Rx, Alpharetta, GA 30005. Includes usage caution to keep out of reach of children and discard after 06/16. Product NDC 61919-139-30 is visible on the label.*
FDA Label Image

Image Description (Molecule)

Image Description (Molecule)
Chemical structure of escitalopram oxalate, the active ingredient in ESCITALOPRAM OXALATE by Direct Rx, showing the molecular arrangement including a cyano group, fluorophenyl group, and dimethylamine side chain attached to the main bicyclic structure, with the oxalate salt represented as C2H2O4.*

* 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.