Ciprofloxacin Tablet
Product Images NDC 43547-688

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 43547-688). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Solco Healthcare Us, 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

C17h18fn3o3•hcl•h2o (Image 01)

C17h18fn3o3•hcl•h2o (Image 01)
Chemical structure of ciprofloxacin hydrochloride monohydrate, showing the molecular arrangement of atoms and bonds including a fluorine-substituted quinolone ring and a piperazine moiety.*
FDA Label Image

C17h18fn3o3 (Image 02)

C17h18fn3o3 (Image 02)
Chemical structure diagram of ciprofloxacin, showing its bicyclic quinolone core with a fluorine atom, piperazine ring, and carboxylic acid group.*
FDA Label Image

250 mg (Image 03)

250 mg (Image 03)
Ciprofloxacin Tablets, USP 250 mg oral tablets packaging label by Solco Healthcare US, LLC. The label includes dosage strength, quantity of 100 tablets, barcode, manufacturing and distribution details, storage instructions, and a notice to dispense the medication guide to patients.*
FDA Label Image

500 mg (Image 04)

500 mg (Image 04)
Label for Ciprofloxacin Tablets, USP 500 mg oral tablets by Solco Healthcare US, LLC. The label shows the NDC 43547-689-10 and indicates the product contains 100 tablets. It includes storage instructions, manufacturer Yiling Pharmaceutical Ltd in China, and distributor information in Somerset, NJ. The label advises referring to the medication guide for dosage and administration.*

* 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.