Escitalopram Oxalate
Product Images NDC 10544-969

3 FDA label images from Blenheim Pharmacal, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Escitalopram Oxalate (NDC 10544-969). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Blenheim Pharmacal, 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

Structure (0bbc78c6 1ba6 4fca 853f E4936d58b08c 01)

Structure (0bbc78c6 1ba6 4fca 853f E4936d58b08c 01)
Chemical structure diagram of Escitalopram Oxalate, depicting its molecular composition with labeled atoms and bonds, including a fluorophenyl group and oxalate moiety (C2H2O4).*
FDA Label Image

Label 10mg 30ct (Label Escitalopram Tabs 10mg Bpi(10544 968 30) Mylan(0378 3856 10) Rev1)

Label 10mg 30ct (Label Escitalopram Tabs 10mg Bpi(10544 968 30) Mylan(0378 3856 10) Rev1)
Packaging label for Escitalopram Tablets USP 10mg by Blenheim Pharmacal, Inc. The label indicates a package of 30 tablets with a prescription-only designation. Storage instructions specify controlled room temperature and keeping the container tightly closed and out of reach of children. The label includes multiple NDC and manufacturing codes and barcodes.*
FDA Label Image

Label 20mg 30ct (Label Escitalopram Tabs 20mg Bpi(10544 969 30) Mylan(0378 3857 10) Rev1)

Label 20mg 30ct (Label Escitalopram Tabs 20mg Bpi(10544 969 30) Mylan(0378 3857 10) Rev1)
Packaging label for Escitalopram Tablets USP 20mg, containing 30 tablets. The label states 'Rx Only' and includes storage instructions to keep at controlled room temperature (20°-25°C) and in a tight, light-resistant container out of reach of children. The label also identifies Blenheim Pharmacal, Inc. as the manufacturer, with the NDC 10544-969-30 and lot and expiration date placeholders shown.*

* 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.