Metaxalone Tablet
Product Images NDC 0904-6831

3 FDA label images from Major Pharmaceuticals · 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 0904-6831). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Major Pharmaceuticals, 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

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Metaxalone 800 mg oral tablets by Major Pharmaceuticals, presented as Unit Dose packaging with 30 tablets per package. The label states the product is prescription only, including dosing information and storage instructions (20° to 25°C with excursions permitted between 15° to 30°C). It also contains manufacturer and distributor details along with a barcode and the NDC number 0904-6831-04.*
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 in blood (ng/mL) over 12 hours following an 800 mg dose under fasted and fed conditions. The x-axis represents time in hours, and the y-axis shows drug concentration. Fed condition shows higher concentrations than fasted, with error bars indicating variability.*
FDA Label Image

Metaxalone 800 mg (Chemical Structure)

Metaxalone 800 mg (Chemical Structure)
Chemical structure of Metaxalone showing its molecular formula with labeled bonds and atom groups including methyl and amide functional groups.*

* 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.