Moxifloxacin Hydrochloride Tablet, Film Coated
Product Images NDC 72789-037

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Moxifloxacin Hydrochloride (NDC 72789-037). 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

72789037 Label (72789037)

Label for MOXIFLOXACIN USP 400 MG tablets from PD-Rx Pharmaceuticals, Inc., Oklahoma City, OK. The label indicates a package size of 10 film-coated oral tablets. It includes the NDC 72789-037-10, lot number B20D03 and expiration date 02/2022. A warning in pink highlights to keep out of reach of children. Dosage instructions are blank with spacing for number of tablets and times per day. The label also includes reorder number 111000 and advises to finish all medication unless directed otherwise.*

FDA Label Image

Figure 1 (Moxifloxacin Fig1)

A line graph comparing plasma concentration (mcg/mL) over time (hours) for oral dose and intravenous (i.v.) dose. The graph shows plasma concentration peaks shortly after dosing and then gradually decreases over 24 hours, illustrating pharmacokinetic profiles for both administration routes.*

FDA Label Image

Structure (Moxifloxacin Str)

Chemical structure of moxifloxacin hydrochloride, the active ingredient in MOXIFLOXACIN HYDROCHLORIDE 400 mg film-coated tablets by PD-Rx Pharmaceuticals, Inc. The diagram shows the molecular framework including key functional groups and the hydrochloride salt notation (*HCl).*

* 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.