Citalopram
Product Images NDC 50436-0917

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Citalopram (NDC 50436-0917). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unit Dose Services, 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

Cita-str1 (Cita Str1)

Chemical structure of citalopram hydrobromide, showing its molecular arrangement with aromatic rings, a nitrile group, fluorine, and a dimethylaminopropyl substituent.*

FDA Label Image

Package Label.principal Disply Panel (20 MG(100's Bottle))

Label for Citalopram Tablets, USP 20 mg by Aurobindo Pharma USA, Inc., showing 100 tablets per container. The label includes storage instructions, dispensing guidelines, and manufacturer information for Aurolife Pharma LLC, Dayton, NJ. It features a barcode and NDC 13107-006-01.*

FDA Label Image

Package Label.principal Disply Panel (30 MG(100's Bottle))

Label for Citalopram Tablets USP 40 mg by Aurobindo Pharma USA, Inc., manufactured by Aurobindo Pharma LLC. The label states it contains 100 tablets, is Rx only, and includes storage instructions and dispensing guidance. The label features the Aurobindo logo and indicates pharmacist dispensing requirements.*

FDA Label Image

Label Image (Rspl50436 0917)

Citalopram Hydrobromide 40 mg tablet blister pack, containing 30 tablets. The label shows the NDC 50436-0917-1 and states it is packaged by Unit Dose Services, LLC, with manufacturing by Aurolife Pharm. Storage instructions recommend keeping it at 20-25°C (68-77°F) in controlled room temperature, with a warning to keep out of reach of children.*

* 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.