Moxifloxacin Tablet, Film Coated
Product Images NDC 33342-322

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Moxifloxacin (NDC 33342-322). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Macleods Pharmaceuticals Limited, 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

Blister Carton (Moxifloxacin 10x10s Carton)

Label for Moxifloxacin Tablets, USP 400 mg by Macleods Pharmaceuticals Limited and Macleods Pharma USA, Inc. It is an oral film-coated tablet available in unit-dose packaging of 100 tablets (10 x 10). The label includes drug name, strength (400 mg), manufacturer and distributor details, a barcode, and pharmacist dispensing instructions.*

FDA Label Image

30s Count (Moxifloxacin 30s Container)

Label for Moxifloxacin Tablets, USP 400 mg film-coated oral tablets manufactured by Macleods Pharmaceuticals Limited. The label includes storage instructions, pharmacist dispensing advice, and manufacturer details including Macleods Pharma USA, Inc. in Princeton, NJ, and packaging info for 30 tablets per container.*

FDA Label Image

Fig (Moxifloxacin Fig1)

A line graph showing plasma concentration (µg/mL) over time (hours) comparing oral dose versus intravenous (I.V.) dose of Moxifloxacin. Both dosing methods exhibit peak plasma concentrations shortly after administration followed by a gradual decline over 24 hours.*

FDA Label Image

Str (Moxifloxacin Structure)

Chemical structure of moxifloxacin as depicted in the image, showing its molecular arrangement including rings, fluorine atom, and functional groups.*

* 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.