Citalopram Tablet, Film Coated
Product Images NDC 0904-6084

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Citalopram (NDC 0904-6084). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Major Pharmaceuticals, 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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Citalopram 40 mg film-coated oral tablets by Major Pharmaceuticals. The label shows unit dose packaging with 100 tablets. It includes NDC 0904-6086-61, pharmacist dispensing instructions, Rx only designation, and storage information. The label also notes the product is for institutional use only and includes manufacturer and distributor details.*

FDA Label Image

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Citalopram 20 mg film-coated tablets packaging label from Major Pharmaceuticals. The label indicates unit dose format with 100 tablets per package. It includes instructions for pharmacists to dispense with a medication guide and states the product is prescription-only. The label shows the NDC number 0904-6085-61, manufacturing and distribution details, and storage conditions.*

FDA Label Image

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Label for Citalopram 10 mg film-coated tablets by Major Pharmaceuticals. The label states 'Unit Dose' with strength 10 mg, prescription use (Rx only), and contains 100 tablets. It includes dispensing instructions, storage conditions (20°-25°C), and manufacturer details for Major Pharmaceuticals and Torrent Pharmaceuticals Ltd. The NDC is 0904-6084-61.*

FDA Label Image

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Chemical structure of citalopram hydrobromide, showing the molecular arrangement including a cyano group, fluorophenyl ring, and dimethylaminopropyl side chain with hydrobromide salt.*

FDA Label Image

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FDA Label Image

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* 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.