Moxifloxacin Hydrochloride Tablet, Film Coated
Product Images NDC 72789-350

View Photos of 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 (NDC 72789-350). 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.

Product Images & Figures Index

FDA Label Image

72789350 Label (72789350)

72789350 Label (72789350)
Label for Moxifloxacin Hydrochloride USP 400 mg film-coated tablets, 10 count, from PD-Rx Pharmaceuticals, Inc. The label includes dosage warnings, storage instructions, and manufacturing details. It shows the NDC number 72789-350-10 and the expiration date 04/2026. The label is printed in English and Spanish and includes a QR code for patient medication guides.*
FDA Label Image

Figure 1 (Moxifloxacin Fig1)

Figure 1 (Moxifloxacin Fig1)
A plasma concentration versus time graph comparing oral and intravenous doses of Moxifloxacin Hydrochloride. The y-axis shows plasma concentration in mcg/mL; the x-axis shows time in hours. Data points for both oral and IV doses show a concentration peak followed by a gradual decline over 24 hours.*
FDA Label Image

Structure (Moxifloxacin Str)

Structure (Moxifloxacin Str)
Chemical structure of Moxifloxacin Hydrochloride, a fluoroquinolone antibiotic compound showing a bicyclic quinolone core with a cyclopropyl group and a fluorine atom, with the hydrochloride salt form indicated.*

* 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.