Ciprofloxacin
Product Images NDC 53401-004

3 FDA label images from Testpak Holding Company · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ciprofloxacin (NDC 53401-004). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Testpak Holding Company, 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

Structural Formula (A9a60b57 445d 4c27 Bdca 5a0cbfb90502 01)

Structural Formula (A9a60b57 445d 4c27 Bdca 5a0cbfb90502 01)
Chemical structure of Ciprofloxacin hydrochloride monohydrate, showing the fluorinated quinolone core with piperazine and cyclopropyl groups, along with the carboxylic acid and ketone functional groups.*
FDA Label Image

Creatinine Clearance Calculation (A9a60b57 445d 4c27 Bdca 5a0cbfb90502 02)

Creatinine Clearance Calculation (A9a60b57 445d 4c27 Bdca 5a0cbfb90502 02)
A text panel showing the formula for calculating creatinine clearance (mL/min), with separate instructions for men and women. The formula uses weight (kg), age, and serum creatinine (mg/dL) values with a correction factor for women.*
FDA Label Image

Principal Display Panel (500 mg Label)

Principal Display Panel (500 mg Label)
Label for Ciprofloxacin 500 mg tablets by Testpak Holding Company. The label states each tablet contains ciprofloxacin hydrochloride equivalent to 500 mg ciprofloxacin, with a package count of 20 tablets. Instructions indicate usual dosage and storage conditions. The label includes manufacturer, distributor information, NDC number 53401-004-20, and usage restrictions.*

* 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.