Metaxalone Tablet
Product Images NDC 71205-326

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 71205-326). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

Structural Formula (Image 1)

Structural Formula (Image 1)
Chemical structure of Metaxalone, showing its molecular arrangement with aromatic and amide functional groups, consistent with the generic drug Metaxalone used as an oral tablet.*
FDA Label Image

Figure 1. Mean (sd) Concentrations Of Metaxalone Following An 800 mg Dose Under Fasted And Fed Conditions (Image 2)

Figure 1. Mean (sd) Concentrations Of Metaxalone Following An 800 mg Dose Under Fasted And Fed Conditions (Image 2)
A line graph showing the mean (SD) concentrations of Metaxalone in ng/mL over 12 hours following an 800 mg dose under fasted and fed conditions. The graph compares concentration levels at various time points with separate curves for fasted and fed states, indicating differences in drug concentration over time.*
FDA Label Image

71205-326-30 (Image 3)

71205-326-30 (Image 3)
Label for Metaxalone 800 mg oral tablets by Proficient Rx LP. The package contains 30 capsule-shaped, scored tablets, each containing 800 mg of Metaxalone. The tablets are white to off-white, inscribed with "31 90" on the scored side and "WPI" on the other. Manufactured by Actavis Laboratories FL, Inc., Fort Lauderdale, FL. Storage instructions specify 20°-25°C (68°-77°F). NDC 71205-326-30.*

* 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.