Escitalopram Oxalate Tablet, Film Coated
Product Images NDC 53746-021

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Escitalopram Oxalate (NDC 53746-021). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Of New York 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

Structural Formula (Escitalopram Tablets Usp 1)

Chemical structure diagram of Escitalopram Oxalate, showing its molecular framework and the oxalate component (C2H2O4).*

FDA Label Image

5 mg 30 Ct Label (Escitalopram Tablets Usp 2)

Label for Escitalopram Tablets, USP 5 mg film-coated oral tablets by Amneal Pharmaceuticals of New York LLC. The label states each tablet contains 6.387 mg escitalopram oxalate (equivalent to 5 mg escitalopram base) and includes dosage and storage instructions. The package contains 30 tablets and includes a barcode and cautions for pharmacists and storage conditions.*

FDA Label Image

10 mg 30 Ct Label (Escitalopram Tablets Usp 3)

Label for Escitalopram Oxalate 10 mg film-coated tablets, USP, containing 30 tablets. Distributed by Amneal Pharmaceuticals of New York LLC, Bridgewater, NJ. Includes dosage strength, dispensing instructions, storage conditions, a barcode, and pharmacy dispensing note. The label is primarily white with purple and black text.*

FDA Label Image

20 mg 30 Ct Label (Escitalopram Tablets Usp 4)

Escitalopram Tablets, USP 20 mg film-coated tablets in a pharmacist label from Amneal Pharmaceuticals of New York LLC. The label includes drug strength, quantity (30 tablets), storage instructions, dosage guidance reference, barcode, and distribution information from Bridgewater, NJ.*

* 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.