Levofloxacin
Product Images NDC 12634-675

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Levofloxacin (NDC 12634-675). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Apotheca 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

Label (675 00)

Levofloxacin 500 mg 10 tablets packaging label from Apotheca Inc. The label includes the product name, strength, quantity, NDC 12634-675-00, instructions to see the insert for full prescribing information, and notes the product is repackaged and distributed by Apotheca, Inc., Phoenix, AZ. Directions advise taking the tablets by mouth as directed by a physician.*

FDA Label Image

Figure2 (Figure2)

A line graph comparing plasma concentration over time in hours for 750 mg Levofloxacin administered orally as a tablet and intravenously via a 90 minute infusion. The y-axis shows plasma concentration (µg/mL) from 0 to 12, and the x-axis shows time from 0 to 36 hours. The intravenous infusion shows a sharp peak at time zero, while the oral tablet shows a gradual peak before both decline over time.*

FDA Label Image

Figure3 (Figure3)

A pharmacokinetic graph showing plasma concentration (µg/mL) over time (hours) for Levofloxacin 500 mg administered orally (p.o.) and intravenously (i.v.). The chart compares plasma levels, illustrating concentration changes up to 36 hours post-dose.*

FDA Label Image

Formula (Formula)

Chemical structure of the active ingredient Levofloxacin, showing its molecular arrangement including fluorine, oxygen, nitrogen groups, and partial hydrate form (1/2 H2O).*

* 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.