Ciprofloxacin Tablet, Film Coated
Product Images NDC 51407-165

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ciprofloxacin (NDC 51407-165). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Golden State Medical Supply, Inc., 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

51407-165-01lb.jpg (51407 165 01lb)

Label for Ciprofloxacin Tablets USP, 500 mg strength, containing 100 tablets. The label includes the NDC number 51407-165-01 and states it is for oral administration. Labeler is Golden State Medical Supply, Inc. Additional information notes to see package insert for dosage and that the product is Rx only.*

FDA Label Image

Chemical Structure (Cip07 0007 01)

Chemical structure diagram of Ciprofloxacin Hydrochloride, showing its molecular framework with labeled atoms and bonds.*

FDA Label Image

Chemical Structure (Cip07 0007 02)

Chemical structure of ciprofloxacin hydrochloride. The diagram shows the molecular arrangement of ciprofloxacin, including its fused ring system and functional groups, consistent with its identity as the active ingredient in Ciprofloxacin 500 mg film-coated tablets by Golden State Medical Supply, Inc.*

FDA Label Image

Figure (Cip07 0007 04)

Packaging label for Ciprofloxacin 500 mg film-coated tablets. The label includes the product name Ciprofloxacin, strength 500 mg, dosage form as film-coated tablets, and highlights the oral route of administration. The labeler is Golden State Medical Supply, Inc., with product NDC 51407-165. The carton likely contains a bottle or multiple tablets.*

* 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.