Escitalopram Tablet, Film Coated
Product Images NDC 51655-149

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 51655-149). 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 149 26 Master Bottle Label Approval Rev A 02 22)

Label (51655 149 26 Master Bottle Label Approval   Rev A 02 22)
Label for Escitalopram Tablets, USP 10 mg by Northwind Health Company, LLC. It indicates 90 film-coated tablets in the container with Rx only status. Storage instructions include keeping at 25°C with permitted excursions, and to store in the original container out of reach of children. The label displays the NDC 51655-149-26 and provides packaging and manufacturing details.*
FDA Label Image

Structural Formula Of Escitalopram Oxalate (Escitalopram Str)

Structural Formula Of Escitalopram Oxalate (Escitalopram Str)
Chemical structure of Escitalopram, illustrating its molecular arrangement including a fluoro-substituted bicyclic ring system and a dimethylaminoethoxy side chain, with an associated water of hydration (C2H4O).*

* 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.