Metaxalone Tablet
Product Images NDC 72789-028

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 Metaxalone (NDC 72789-028). 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

72789028 Label (72789028)

72789028 Label (72789028)
Metaxalone USP 800 mg oral tablets carton and label by PD-Rx Pharmaceuticals, Inc. The label shows NDC 72789-028-30 and contains 30 tablets. It includes warning text about alcohol use, drowsiness, and keeping out of children's reach, as well as lot number C22B31 and expiration date 03/2024. The label also features a barcode and QR code.*
FDA Label Image

Figure 1 (Mean (SD) Concentrations of Metaxalone following an 800 mg Dose under Fasted and Fed Conditions.)

Figure 1 (Mean (SD) Concentrations of Metaxalone following an 800 mg Dose under Fasted and Fed Conditions.)
A line graph showing mean concentrations of Metaxalone 800 mg over a 12-hour period comparing fasted and fed conditions. The y-axis represents concentration in ng/mL, with higher values under fed conditions. The x-axis represents time in hours, illustrating concentration changes post-dose for both conditions, including standard deviation error bars.*
FDA Label Image

Metaxalone 800 mg (Chemical Structure)

Metaxalone 800 mg (Chemical Structure)
Chemical structure of Metaxalone, showing its molecular arrangement including a benzene ring with two methyl groups and the carbamate functional group.*

* 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.