Levofloxacin Tablet, Film Coated
Product Images NDC 68071-3093

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Levofloxacin (NDC 68071-3093). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare 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

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Label for Levofloxacin 250 mg film-coated tablets by NuCare Pharmaceuticals, Inc. The label indicates a package of 30 tablets with prescription use only. It includes manufacturing information by Hetero Labs Limited in India, barcode, and warnings to keep out of reach of children. Storage instructions specify controlled temperature of 68-77°F.*

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Levofloxacinaddress1 (Levofloxacinaddress1)

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Levofloxacinfigure1 (Levofloxacinfigure1)

Chemical structure diagram of Levofloxacin, showing the molecular arrangement including fluorine atom, methyl groups, and other characteristic rings and bonds typical of the antibiotic molecule. The structure includes a half water molecule (½ H2O) notation indicating a hydrate form.*

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A line graph showing plasma concentration (in µg/mL) over time (hours) for 750 mg doses of Levofloxacin administered orally as a tablet and intravenously as a 90-minute infusion. The graph compares the plasma concentration profiles for both administration routes over a 36-hour period.*

FDA Label Image

Levofloxacinfigure3 (Levofloxacinfigure3)

A pharmacokinetic graph showing plasma concentration (ng/mL) on the y-axis versus time (hours) on the x-axis. The chart compares plasma concentrations over time for 500 mg Levofloxacin administered orally (p.o.) and intravenously (i.v.).*

* 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.