Escitalopram Oxalate Tablet, Film Coated
Product Images NDC 72603-150

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Escitalopram Oxalate (NDC 72603-150). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rxllc, 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

159 (Escitalopram)

Chemical structure of escitalopram oxalate, showing its molecular arrangement including aromatic rings, fluorine, and oxalate moiety.*

FDA Label Image

222 (Escitalopram Tab 10 mg 1000s)

Label for Escitalopram Tablets, USP 10 mg, film-coated oral tablets. The label includes storage instructions, dispensing guidance, manufacturer information (Macleods Pharmaceuticals Ltd and NorthStar Rx LLC), and a barcode. The package contains 1000 tablets and highlights that the medication guide should be provided separately to each patient.*

FDA Label Image

444 (Escitalopram Tab 20 mg 1000s)

Label for Escitalopram Tablets USP 20 mg film-coated tablets by NorthStar RxLLC, packaged as 1000 tablets. The label states each tablet contains escitalopram oxalate equivalent to 20 mg escitalopram, storage instructions, barcode, and manufacturer information including NorthStar Rx LLC and Macleods Pharmaceuticals Ltd., India.*

FDA Label Image

111 (Escitalopram Tab 5 mg 1000s)

Label for Escitalopram Tablets, USP 5 mg film coated tablets, in a package containing 1000 tablets. The label includes storage instructions, dosage guidance to see prescribing information, barcodes, and manufacturer details for NorthStar Rx LLC and Macleods Pharmaceuticals Ltd. It also indicates the medication guide is available online or by phone.*

* 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.