Ciprofloxacin
Product Images NDC 51655-118

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ciprofloxacin (NDC 51655-118). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Pharmaceuticals, 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

51655-118-20 (51655 118 20)

Label for ciprofloxacin 500 mg tablets, showing a package count of 20 tablets. The label includes the NDC number 51655-0118-20 and details such as lot number UB3066 1 and an expiration date of 09/17. Manufacturer is Unique Pharmaceutical Laboratories, with manufacturing in Mumbai. Distributed by Northwind Pharmaceuticals, LLC in Indianapolis, IN. The label includes storage instructions and a note that the product is Rx only.*

FDA Label Image

51655-118-53 (51655 118 53)

Packaging label for ciprofloxacin 500mg tablets. The label indicates a quantity of 10 tablets in the package. It includes the NDC number 51655-0118-53, manufacturing details from Unique Pharmaceutical Laboratories, Mumbai, India, and distribution by Northwind Pharmaceuticals, LLC, Indianapolis, IN. The label specifies storage below 86F (30C) and states Rx Only.*

FDA Label Image

51655-118-84 (51655 118 84)

Label for ciprofloxacin 500 mg tablets, package of 14 tablets. The label includes NDC 51655-0118-84 and indicates it is prescription only. Manufactured by Unique Pharmaceutical Laboratories, Mumbai, India, and distributed by Northwind Pharmaceuticals, LLC, Indianapolis, IN. Storage instructions specify below 86°F (30°C).*

* 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.