Ciprofloxacin
Product Images NDC 70934-965

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ciprofloxacin (NDC 70934-965). 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 965 20 Master Bottle Label Approval Rev A 04 22)

Label (70934 965 20 Master Bottle Label Approval   Rev A 04 22)
Label for Ciprofloxacin Tablets USP 500 mg by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The label indicates the package contains 20 tablets, with storage instructions and regulatory information including NDC 70934-965-20. It also provides handling and dosage directions, and lot and expiration details are included.*
FDA Label Image

Chemical Structure (Cip07 0007 01)

Chemical Structure (Cip07 0007 01)
Chemical structure of Ciprofloxacin showing its molecular configuration with characteristic rings and functional groups as represented in the diagram.*
FDA Label Image

Chemical Structure (Cip07 0007 02)

Chemical Structure (Cip07 0007 02)
Chemical structure of Ciprofloxacin, showing its bicyclic quinolone core with a carboxyl group and piperazinyl moiety as part of its molecular structure.*
FDA Label Image

Figure (Cip07 0007 04)

Figure (Cip07 0007 04)
Packaging label for Ciprofloxacin tablets from Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The label shows Ciprofloxacin in a white and orange container with black and orange text highlighting the product name and labeler information. Other label details are not fully legible.*

* 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.