Metaxalone
Product Images NDC 21695-585

3 FDA label images from Rebel Distributors Corp. · 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 21695-585). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp., 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

Chemical Structure (21618014 77c1 4a35 Acca Cd5678d7bb89 01)

Chemical Structure (21618014 77c1 4a35 Acca Cd5678d7bb89 01)
Chemical structure diagram of Metaxalone, showing its molecular arrangement including methyl groups, an oxygen bridge, and a heterocyclic ring with nitrogen and carbonyl groups.*
FDA Label Image

Figure 1 (21618014 77c1 4a35 Acca Cd5678d7bb89 02)

Figure 1 (21618014 77c1 4a35 Acca Cd5678d7bb89 02)
A line graph showing Metaxalone concentration (ng/mL) over time (hours) comparing fasted and fed states. Concentration rises, peaks around 3-4 hours, then declines up to 12 hours, with higher concentrations observed in the fed state across most time points. Error bars represent variability.*
FDA Label Image

Metaxalone 800mg (21618014 77c1 4a35 Acca Cd5678d7bb89 03)

Metaxalone 800mg (21618014 77c1 4a35 Acca Cd5678d7bb89 03)
Metaxalone 800 mg tablets label showing a package of 90 tablets. The label indicates it is a prescription-only product with the NDC 21695-585-90. It is packaged by Physician Partner, a division of Rebel Distributors Corp., and the manufacturer is Sandoz Inc., Princeton, NJ. Instructions for storage at controlled room temperature 15°-30°C (59°-86°F) and a warning to keep the medication out of reach of children are included.*

* 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.