Ciprofloxacin Tablet, Film Coated
Product Images NDC 51655-216

View Photos of 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 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 (51655 216 87   Rev A 03 23)
This is a description of a medication containing Ciprofloxacin Hydrochloride Monohydrate in the form of tablets, USP with each tablet having 500mg of the active ingredient. The tablets come in an original container with six tablets in it. The dosage prescription is advised by reading the package insert. The tablets should be stored in a controlled room with temperatures between 15°-30°C (59°-86°F). This medication is meant for prescription only, and should not be accessible to children. There is a lot number and expiration date for the medication. Repackaged by Northwind Pharmaceuticals, this particular medication is a repackaged version from Aurobindo Phamma USA Inc. Its NDC code is 51655-216-87, GTIN: 00351655216873 and LCN#: 00.*
FDA Label Image

Chemical Structure (Ciprofloxacin Str1)

FDA Label Image

Chemical Structure (Ciprofloxacin Str2)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.