Metaxalone Tablet
Product Images NDC 51655-792

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 51655-792). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, Llc, 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

Label (51655 792 20 Master Bottle Label Approval Rev A 01 22)

Label (51655 792 20 Master Bottle Label Approval   Rev A 01 22)
Metaxalone 800 mg tablets label showing 20 tablets in the package. The label states the product is for prescription use only, with storage instructions and temperature guidelines. The labeler is Northwind Health Company, LLC. The label includes NDC number 51655-792-20 and batch coding details.*
FDA Label Image

Structural Formula (Metaxalone Tablets 1)

Structural Formula (Metaxalone Tablets 1)
Chemical structure of Metaxalone showing its molecular framework with two methyl groups attached to a benzene ring linked via an ether and ester functional groups to an amide-containing side chain.*
FDA Label Image

Figure 1 (Metaxalone Tablets 2)

Figure 1 (Metaxalone Tablets 2)
A line graph showing the mean concentrations (ng/mL) of Metaxalone after an 800 mg oral dose under fasted and fed conditions over 12 hours. The y-axis represents drug concentration, while the x-axis shows time in hours. Two lines compare fasted (lower concentration) and fed (higher concentration) states with standard deviation error bars.*

* 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.