Escitalopram Tablet, Film Coated
Product Images NDC 55154-7288

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Escitalopram (NDC 55154-7288). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cardinal Health 107, 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

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Afe9596b 3231 4248 891c 5f2f9e6dd83a 01
Chemical structure diagram of escitalopram, showing its molecular configuration including aromatic rings, a fluorine and nitrogen atom, and an oxalate moiety indicated by the formula C2H2O4.*
FDA Label Image

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FDA Label Image

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FDA Label Image

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B26dcf34 Cb2c 4d69 94a9 Bef595c900c7 00
Escitalopram Tablets, USP 20 mg tablet label showing NDC 55154-7288-0. The label states that each film-coated tablet contains escitalopram oxalate equivalent to 20 mg escitalopram. Package contains 10 tablets. It includes storage instructions, warnings, and manufacturing information by Torrent Pharmaceuticals Ltd. and distribution by Cardinal Health.*
FDA Label Image

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B26dcf34 Cb2c 4d69 94a9 Bef595c900c7 01
Escitalopram tablets USP 10 mg label displaying a package of 10 tablets. The film-coated tablets contain escitalopram oxalate equivalent to 10 mg escitalopram. The label includes storage instructions, dosage guidance referral, and a warning about package child resistance and institutional use. Manufactured by Torrent Pharmaceuticals Ltd, India, and distributed by Cardinal Health and Major Pharmaceuticals in the USA.*

* 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.