Metaxalone Tablet
Product Images NDC 61919-832

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Metaxalone (NDC 61919-832). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct Rx, 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

091 (091 30)

METAXALONE 800 mg tablet carton label with 30 tablets, labeled as generic for Skelaxin. The label shows the strength as 800 mg per tablet, packaging information by Direct Rx, and includes warnings such as "May cause drowsiness or dizziness." The label also displays the National Drug Code (NDC) numbers and lot/expiration date details.*

FDA Label Image

832 90

METAXALONE 800 mg tablet label showing packaging for 90 tablets. It specifies the product is generic for SKELAXIN and each tablet contains 800 mg of Metaxalone, USP. The label includes lot number 20MA1910 and discard date 7/31/20. Packaged and distributed by DIRECT RX. Additional text lists NDC 61919-832-90 and barcode information.*

* 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.