Moxifloxacin Hydrochloride Tablet, Film Coated
Product Images NDC 65862-603

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Moxifloxacin Hydrochloride (NDC 65862-603). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma 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

Figure 1 (Moxifloxacin Fig1)

A line graph showing plasma concentration (mcg/mL) of a drug over time (hours) comparing oral and intravenous (i.v.) doses. The graph illustrates the drug's concentration peak and decline within 24 hours post-dose for both administration routes.*

FDA Label Image

Figure2 (Moxifloxacin Fig2)

Label for Moxifloxacin Tablets USP 400 mg film-coated tablets by Aurobindo Pharma Limited, showing the NDC 65862-603-30. The label indicates each tablet contains 400 mg moxifloxacin, and includes storage instructions, distribution details by Aurobindo Pharma USA, Inc., and packaging of 30 tablets. It features dosage and pharmacist dispensing instructions along with barcode and manufacturing code.*

FDA Label Image

Figure 3 (Moxifloxacin Fig3)

Label for Moxifloxacin Tablets, USP 400 mg film-coated tablets by Aurobindo Pharma. The packaging indicates 50 (5 x 10) unit-dose tablets. NDC 65862-603-55 is displayed along with pharmacist instructions and storage conditions. Distributed by Aurobindo Pharma USA, Inc., made in India.*

FDA Label Image

Structure (Moxifloxacin Str)

Chemical structure of Moxifloxacin Hydrochloride, showing atoms and bonds including a fluorine-substituted quinolone core, attached cyclopropyl and methoxy groups, and a hydrochloride indicated by *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.