Ciprofloxacin Tablet
Product Images NDC 80425-0492

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ciprofloxacin (NDC 80425-0492). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Of Tennessee, 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

Ciprofloxacin 500mg #20 (Ciprofloxacin 500mg 80425 0492 01)

Label for Ciprofloxacin 500 mg tablet, oral dosage form, manufactured by Advanced Rx of Tennessee, LLC. The label includes a comparison to Cipro, NDC 80425-0492-01, lot number and expiration date fields, storage instructions at 20-25°C (68-77°F), and indicates prescription use only. The label also shows a barcode and the product count of 20 tablets.*

FDA Label Image

Ciprofloxacin 500mg #30 (Ciprofloxacin 500mg 80425 0492 02)

Label for Ciprofloxacin 500 mg oral tablets from Advanced Rx of Tennessee, LLC. The label includes dosage strength, NDC 80425-0492, lot number placeholder, expiration date 12/31/2026, and comparison to Cipro brand. Storage instructions for 20°-25°C (68°-77°F) and a barcode are visible.*

FDA Label Image

C17h18fn3o3•hcl•h2o (Image 01)

Chemical structure of ciprofloxacin hydrochloride monohydrate, showing the molecular composition with fluorine, oxygen, nitrogen, and other atoms arranged in a bicyclic quinolone framework.*

FDA Label Image

C17h18fn3o3 (Image 02)

Chemical structure diagram of ciprofloxacin, illustrating its core quinolone ring system with attached functional groups including a carboxyl group, fluorine atom, and a piperazine ring. This structure represents the active ingredient ciprofloxacin.*

* 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.