Escitalopram Tablet, Film Coated
Product Images NDC 51655-236

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 51655-236). 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 236 52 Master Bottle Label Approval Rev A 05 21)

Label (51655 236 52 Master Bottle Label Approval   Rev A 05 21)
This is a description of a drug called Escitalopram. It comes in the form of USP Tablets, and is available in 20mg strength. It has a NDC number of 51655-236-52 and the manufacturer is Accord Healthcare Inc, but it has been repackaged by Northwind Pharmaceuticals. The tablets should be kept at room temperature, and out of reach of children. The package includes dosage information and a package insert, and each coated tablet contains ram oxalate, USP equivalent to an unknown amount. The expiration date is listed as 00/00/0000, and the lot number is 0000000000.*
FDA Label Image

Structural Formula Of Escitalopram Oxalate (Escitalopram Str)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.