Ciprofloxacin
Product Images NDC 70934-934

3 FDA label images from Denton Pharma, Inc. Dba Northwind Pharmaceuticals · 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 70934-934). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Denton Pharma, Inc. Dba Northwind Pharmaceuticals, 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 (70934 934 20 Master Bottle Label Approval Rev A 12 21)

Label (70934 934 20 Master Bottle Label Approval   Rev A 12 21)
Label for Ciprofloxacin Tablets USP 500 mg by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The label shows the product NDC 70934-934-20, indicating a 20-count tablet package. Instructions include storing at 20° to 25°C (68° to 77°F) and keeping the container tightly closed and out of reach of children, with a reference to see the package insert for dosage information.*
FDA Label Image

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

Ciprofloxacin Hydrochloride Chemical Structure (Ciprofloxacin Tablets  Mfd By Hikma 1)
Chemical structure diagram of Ciprofloxacin hydrochloride monohydrate, showing the fluorinated quinolone core, cyclopropyl group, piperazine ring, and associated hydrochloride and water components.*
FDA Label Image

Ciprofloxacin Chemical Structure (Ciprofloxacin Tablets Mfd By Hikma 2)

Ciprofloxacin Chemical Structure (Ciprofloxacin Tablets  Mfd By Hikma 2)
Chemical structure of Ciprofloxacin showing its fused ring system including a quinolone core, a cyclopropyl group, a fluorine substituent, a carboxylic acid group, and a piperazine ring.*

* 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.