Citalopram Hydrobromide Tablet, Film Coated
Product Images NDC 51655-043

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Citalopram Hydrobromide (NDC 51655-043). 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 043 52 Rev B 04 21)

Label for Citalopram Tablets USP 10 mg, film-coated oral tablets, containing 30 tablets. Label includes storage instructions, Rx only designation, and repackaging information by Northwind Pharmaceuticals. The NDC number 51655-043-52 is displayed, along with dosage and lot details.*

FDA Label Image

Image (B35147fd 7d3d 47bc Beca B3a7c3762ed1 01)

Chemical structure of the active ingredient Citalopram Hydrobromide, showing its molecular arrangement including aromatic rings, fluorine, and a hydrobromide group.*

FDA Label Image

Logo (B35147fd 7d3d 47bc Beca B3a7c3762ed1 02)

FDA Label Image

Logo (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.