Ciprofloxacin Tablet
Product Images NDC 76420-929

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ciprofloxacin (NDC 76420-929). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Asclemed Usa, 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

C17h18fn3o3•hcl•h2o (Image 01)

Chemical structure diagram of ciprofloxacin hydrochloride monohydrate. The diagram displays the molecular framework, including fluorine, nitrogen, oxygen, and carboxyl functional groups characteristic of ciprofloxacin.*

FDA Label Image

C17h18fn3o3 (Image 02)

Chemical structure of ciprofloxacin, showing its core quinolone ring with fluorine and carboxylic acid functional groups. The diagram includes atom labels and bond connectivity representing the molecular structure of ciprofloxacin.*

FDA Label Image

250 (Label 250mg)

Multiple packaging labels for Ciprofloxacin Tablets USP 250 mg by Enovachem Pharmaceuticals. Labels include various quantities: 20, 30, 60, 90, and 100 tablets. Each label features the NDC numbers, distributor Solco Healthcare US LLC, and storage instructions. Labels indicate prescription status with a caution about dispensing without prescription.*

FDA Label Image

Label (Label 500mg)

Labels for Ciprofloxacin Tablets USP 500 mg by Enovachem Pharmaceuticals, distributed by Solco Healthcare US, LLC. Multiple NDCs correspond to various package quantities: 20, 30, 60, 90 tablets, and relabeled versions with quantities of 100 and 500 tablets. Labels feature lot, expiration date, and drug status RX, with instructions for storage and prescription dispensing.*

* 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.