Ciprofloxacin Tablet, Film Coated
Product Images NDC 43063-547

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ciprofloxacin (NDC 43063-547). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx Pharmaceuticals, 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

Image (43063547)

Label for Ciprofloxacin Tablets USP 500 mg oral film-coated tablets. The package contains 100 tablets. Marketed and packaged by PD-Rx Pharmaceuticals, Inc., and manufactured by Carlsbad Technology, Inc. Storage instructions indicate controlled room temperature (20°C to 25°C) with permitted excursions. The label includes a barcode, NDC 43063-547-01, and states Rx only with instructions for pharmacists to dispense with a medication guide.*

FDA Label Image

Cip07 0007 01

Chemical structure of Ciprofloxacin, depicted as a detailed molecular diagram showing its atomic arrangement and bonds, consistent with the generic drug Ciprofloxacin.*

FDA Label Image

Cip07 0007 02

Chemical structure of ciprofloxacin, showing its molecular framework including fluorine, nitrogen-containing rings, and carboxylic acid group, consistent with the active ingredient ciprofloxacin used in oral tablets.*

FDA Label Image

Cip07 0007 04

Ciprofloxacin 500 mg film-coated tablets package from PD-Rx Pharmaceuticals, Inc. The image shows a blister card containing 10 round, white tablets arranged in two rows of five. The packaging includes printed text with the product name, strength, and other regulatory information on the surrounding foil backing.*

* 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.