Ciprofloxacin Tablet, Film Coated
Product Images NDC 51655-216

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ciprofloxacin (NDC 51655-216). 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 216 87 Rev A 03 23)

Label for Ciprofloxacin Tablets USP 500 mg in a package of 6 tablets. The film-coated oral tablets are labeled as prescription only and include storage instructions between 20°-25°C with permitted excursions. The label identifies Northwind Pharmaceuticals as the repackager and includes barcodes, lot number, expiration date, and other product traceability details.*

FDA Label Image

Chemical Structure (Ciprofloxacin Str1)

Chemical structure diagram of Ciprofloxacin Hydrochloride, showing the molecular arrangement with labeled atoms and bonds as part of the active ingredient in the drug Ciprofloxacin 500 mg film-coated tablets by Northwind Health Company, LLC.*

FDA Label Image

Chemical Structure (Ciprofloxacin Str2)

Chemical structure of Ciprofloxacin Hydrochloride, showing its bicyclic quinolone core with a fluorine atom, a carboxylic acid group, and a piperazine ring attached to the core structure.*

* 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.