Levofloxacin
Product Images NDC 17856-0286

3 FDA label images from Atlantic Biologicals Corp. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Levofloxacin (NDC 17856-0286). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Atlantic Biologicals Corp., 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

Levofloxacin Label (17856 0286 01 Label)

Levofloxacin Label (17856 0286 01 Label)
Levofloxacin oral solution 250 mg per 10 mL unit dose cup labeled with NDC 17856-0286-01 from Atlantic Biologicals Corp. The label includes dosage information (10 mL per cup), storage instructions (25°C with allowable excursions), manufacturer (Hi-Tech Pharmacol Co., Inc.), repackager, and distributor details. Contact information for questions is provided along with a barcode.*
FDA Label Image

Chemical Structure (Image 01)

Chemical Structure (Image 01)
Chemical structure of Levofloxacin with hydrate notation. The structure displays the core bicyclic quinolone framework linked to a fluorine atom and a piperazine ring, including functional groups such as ketone and carboxylic acid.*
FDA Label Image

Figure 2 And 3 (Image 02)

Figure 2 And 3 (Image 02)
Two line graphs showing mean Levofloxacin plasma concentration (μg/mL) over time (hours). The left graph compares 750 mg tablet oral versus 750 mg intravenous (90-minute infusion). The right graph compares 500 mg tablet oral versus 500 mg intravenous. Both show plasma concentration decreasing over 36 hours with IV administration peaking earlier and higher.*

* 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.