Escitalopram Tablet, Film Coated
Product Images NDC 72189-451

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Escitalopram (NDC 72189-451). 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

72189-451-30 (72189 0451 30)

72189-451-30 (72189 0451 30)
Escitalopram 20 mg film-coated tablets, packaged with 30 tablets per container. The label indicates the product is a generic equivalent for Lexapro, with Escitalopram oxalate as the active ingredient equivalent to 20 mg Escitalopram. Distributed by Direct Rx, the lot number is SAMPLE with an expiration date of November 22, 2025. The label includes the NDC 72189-451-30 and manufacturer details.*
FDA Label Image

72189-451-60 (72189 451 60)

72189-451-60 (72189 451 60)
Escitalopram 20 mg film-coated tablets, 60 count, labeled as a generic for Lexapro. The label includes dosage strength, tablet count, lot number, expiration date, and packaging details by Direct Rx. The label also displays multiple sub-labels with identical product information and manufacturing NDC codes.*

* 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.