Metaxalone
Product Images NDC 10544-002

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Metaxalone (NDC 10544-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Blenheim Pharmacal, 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.

FDA Label Image

Bottle Label (10544 002 20 64720 321 10)

Bottle Label (10544 002 20   64720 321 10)
Metaxalone Tablets, 800 mg label for a package containing 20 tablets. The label specifies prescription use only with storage instructions at controlled room temperature in a light-resistant container. The product is labeled by Blenheim Pharmacal, Inc., with NDC 10544-002-20 and lot number and expiration date fields present but not filled in.*
FDA Label Image

Molecular Structure (Metaxalone Tablets 800 mg 1)

Molecular Structure (Metaxalone Tablets 800 mg 1)
Chemical structure diagram of Metaxalone showing its molecular framework including its aromatic ring, ether linkage, and amide group.*
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 depicting mean concentrations of Metaxalone in nanograms per milliliter over time in hours following an 800 mg dose under fasted and fed conditions. The graph shows two curves: one for fasted conditions marked with open circles and another for fed conditions marked with closed circles, each with error bars representing standard deviation.*
FDA Label Image

Corepharma Logo (Metaxalone Tablets 800 mg 3)

* 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.