Moxifloxacin Hydrochloride Tablets, 400 Mg Tablet, Film Coated
Product Images NDC 72789-080

3 FDA label images from Pd-rx Pharmaceuticals, Inc. · 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 Moxifloxacin Hydrochloride Tablets, 400 Mg (NDC 72789-080). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx 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

Structure (Structure)

Structure (Structure)
Chemical structure of moxifloxacin hydrochloride, the active ingredient in Moxifloxacin Hydrochloride Tablets 400 mg by PD-Rx Pharmaceuticals, Inc.*
FDA Label Image

Fig01 (Figure1)

Fig01 (Figure1)
A line graph showing plasma concentration of Moxifloxacin Hydrochloride in mcg/mL over time in hours up to 24 hours. Two curves compare concentrations following oral dose and intravenous (i.v.) dose administration, with both showing a peak near the start and subsequent decline over time.*
FDA Label Image

72789080 Label (72789080)

72789080 Label (72789080)
Label for Moxifloxacin USP 400 mg tablets, containing 10 film-coated tablets. The label indicates the product should be dispensed in a tight/light resistant container and carries warnings about keeping out of children's reach. Manufacturer and packager details include MSN Laboratories Pvt Ltd, India, and PD-Rx Pharmaceuticals, Inc., Oklahoma City, OK. The label features barcodes and instructions to affix additional labels.*

* 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.