Ciprofloxacin Tablet, Film Coated
Product Images NDC 72789-124

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ciprofloxacin (NDC 72789-124). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx Pharmaceuticals, Inc., 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

72789124 Label (72789124)

Label for Ciprofloxacin Tablets USP 250 mg by PD-Rx Pharmaceuticals, Inc. The label indicates a package of 100 film-coated tablets. It includes storage instructions, a barcode, and states the product is for prescription use only. Manufactured by Hikma Pharmaceuticals in Jordan.*

FDA Label Image

72789125 Label (72789125)

Ciprofloxacin 750 mg tablets USP film-coated oral tablets label by PD-Rx Pharmaceuticals, Inc. This label indicates a package size of 50 tablets. It includes storage instructions, barcode, and packaging information showing it is marketed by PD-Rx Pharmaceuticals, Inc. and manufactured by Hikma Pharmaceuticals, Amman, Jordan. The label states 'Rx Only' and features a National Drug Code (NDC) of 72789-125-50.*

FDA Label Image

Ciprofloxacin Hydrochloride Chemical Structure (Ciprofloxacin Tablets Mfd By Hikma 1)

Chemical structure diagram of Ciprofloxacin hydrochloride monohydrate, showing its molecular components including a fluorine-substituted quinolone ring, piperazine moiety, and associated hydrochloride and water molecules.*

FDA Label Image

Ciprofloxacin Chemical Structure (Ciprofloxacin Tablets Mfd By Hikma 2)

Chemical structure of Ciprofloxacin, showing rings and functional groups labeled with positions and including elements such as fluorine, nitrogen, oxygen, and carboxyl group.*

* 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.