Citalopram Hydrobromide
Product Images NDC 53808-0225

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Citalopram Hydrobromide (NDC 53808-0225). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by State Of Florida Doh Central Pharmacy, 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 (Citalopram 10mg(torrent))

Label for Citalopram Hydrobromide 10 mg tablets, prescription only, quantity of 30 tablets. The label shows Lot number B8559001, an expiration date of June 2010, and indicates packaging by the State of Florida DOH Central Pharmacy in Tallahassee, FL 32304. A barcode and UPC number 313668009057 are also visible.*

FDA Label Image

Label (Citalopram 20mg(torrent))

Label for Citalopram 20 mg tablets, quantity of 30, packaged by DCH Central Pharmacy in Tallahassee, FL. The label includes lot number 188477A, expiration date 09/30/2010, and a UPC barcode with number 313566010053. The label states "RX Only."*

FDA Label Image

Image (Citalopram Figure 01)

Chemical structure of Citalopram Hydrobromide showing its molecular framework with key functional groups and bromide ion indicated.*

FDA Label Image

Logo (Citalopram Figure 02)

The image shows a vial of Citalopram Hydrobromide injection, labeled with the proprietary name and the labeler State of Florida DOH Central Pharmacy. The vial contains clear liquid and has a printed label with product information and a barcode.*

* 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.