Levofloxacin Solution
Product Images NDC 0527-1948

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Levofloxacin (NDC 0527-1948). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lannett Company, 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

Levo-molec-struc (Levofloxacin Oral Solution Usp 1)

Chemical structure of Levofloxacin showing its molecular components, including a fluorine atom, oxygen, nitrogen atoms, methyl group, carboxyl group, and a half molecule of water (hydration).*

FDA Label Image

Fig2 (Levofloxacin Oral Solution Usp 2)

A pharmacokinetic curve showing plasma concentration (µg/mL) over time (hours) comparing 750 mg Levofloxacin administered as an oral tablet versus a 90-minute intravenous infusion. Both administration routes display peak plasma concentrations soon after dosing, followed by a gradual decline over 36 hours.*

FDA Label Image

Fig3 (Levofloxacin Oral Solution Usp 3)

A line graph showing plasma concentration (µg/mL) over time (hours) for Levofloxacin 500 mg administered orally (p.o.) as a tablet and intravenously (i.v.). The graph compares blood plasma levels for both administration routes across 36 hours, illustrating concentration peaks and declines.*

FDA Label Image

100 mL Carton (Levofloxacin Oral Solution Usp 4)

Packaging label for Levofloxacin Oral Solution USP 25 mg/mL, a prescription oral solution distributed by Lannett Company, LLC. The label includes dosage strength, NDC number 0527-1948-66, storage instructions, pharmacist dispensing information, and volume of 100 mL. The design features blue and white colors with Lannett branding and a barcode.*

* 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.