Citalopram Tablet, Film Coated
Product Images NDC 51655-680

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 51655-680). 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 680 52 Master Bottle Label Approval Rev A 02 22)

Label (51655 680 52 Master Bottle Label Approval   Rev A 02 22)
Citalopram Tablets USP 20 mg film-coated tablets label showing a 30-tablet count for prescription use only. The label includes storage instructions to keep at controlled room temperature (68°-77°F) with permitted excursions, and warnings to keep out of reach of children and to store in the original container. The labeler is Northwind Health Company, LLC.*
FDA Label Image

Chemical Structure (Citalopram Str)

Chemical Structure (Citalopram Str)
Chemical structure diagram of Citalopram Hydrobromide, showing labeled atoms and bonds characteristic of the molecule.*

* 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.