Escitalopram Tablet, Film Coated
Product Images NDC 51655-449

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 51655-449). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, Llc, 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

Label (51655 449 52 Master Bottle Label Approval Rev A 10 20)

Label (51655 449 52 Master Bottle Label Approval   Rev A 10 20)
Label for Escitalopram Tablets, USP 10 mg film-coated tablets. The package contains 30 tablets and is labeled for prescription use only. Storage instructions specify keeping the product at 25°C (77°F) with permitted excursions between 15°-30°C (59°-86°F). Manufactured and repackaged by Northwind Pharmaceuticals, the label includes NDC 51655-449 and cautions to keep out of reach of children and store in the original container.*
FDA Label Image

Structural Formula Of Escitalopram Oxalate (Escitalopram Str)

Structural Formula Of Escitalopram Oxalate (Escitalopram Str)
Chemical structure of escitalopram, showing its molecular arrangement including fluorophenyl, oxalate, and dimethylamino groups, along with a hydrate component (•C2H4O2).*

* 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.