Citalopram Tablet, Film Coated
Product Images NDC 51655-605

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Citalopram (NDC 51655-605). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, 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

Label (51655 605 52 Master Bottle Label Approval Rev A 02 21)

Label (51655 605 52 Master Bottle Label Approval   Rev A 02 21)
Label for Citalopram tablets, USP 10 mg oral film-coated tablets. The label indicates a package of 30 tablets, prescription only, manufactured by Northwind Health Company, LLC. It includes storage instructions and dosage guidance to see the package insert. The NDC is 51655-605-52.*
FDA Label Image

Chemical Structure (Citalopram Str)

Chemical Structure (Citalopram Str)
Chemical structure of Citalopram Hydrobromide, showing its molecular arrangement including aromatic rings and functional groups as depicted in the image.*

* 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.