Citalopram Tablet, Film Coated
Product Images NDC 51655-667

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Citalopram (NDC 51655-667). 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

51655 664 25 Master Bottle Label Approval Rev A 12 20

Label for Citalopram Tablets USP 20 mg, film-coated oral tablets. The package contains 60 tablets and is marked Rx Only. The label includes storage instructions, repackaging information by Northwind Pharmaceuticals, and identifiers such as NDC 51655-664-25. The label specifies the active ingredient as citalopram hydrobromide, equivalent to 20 mg citalopram base.*

FDA Label Image

51655 667 52 Master Bottle Label Approval Rev A 01 21

Label for Citalopram Tablets, USP 40 mg oral film-coated tablets. The package contains 30 tablets and is labeled Rx Only. The label includes storage instructions, barcodes, and repackaging information from Northwind Pharmaceuticals. The manufacturer or labeler is Northwind Health Company, LLC.*

FDA Label Image

B35147fd 7d3d 47bc Beca B3a7c3762ed1 01

Chemical structure of Citalopram, showing its molecular arrangement including a fluorophenyl group, nitrile group, and a dimethylamino propyl side chain with associated hydrobromide salt (HBr).*

FDA Label Image

B35147fd 7d3d 47bc Beca B3a7c3762ed1 02

FDA Label Image

B35147fd 7d3d 47bc Beca B3a7c3762ed1 03

* 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.