Escitalopram Oxalate Tablet, Film Coated
Product Images NDC 43063-761

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Escitalopram Oxalate (NDC 43063-761). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx Pharmaceuticals, Inc., 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

Image (43063761)

Packaging label for escitalopram oxalate USP 10 mg film-coated tablets, containing 30 tablets per bottle. The label shows the NDC number 43063-761-30 and is manufactured by PD-Rx Pharmaceuticals, Inc., Oklahoma City, OK. It includes lot number C22B15 and expiration date 03/2023, with dosing instructions left blank for prescription fill-in. The label also carries safety warnings and a barcode.*

FDA Label Image

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Chemical structure diagram of escitalopram oxalate, the active ingredient in the product, showing the molecular arrangement including the oxalate moiety (C2H2O4).*

* 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.