Metaxalone Tablet
Product Images NDC 80425-0580

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Metaxalone (NDC 80425-0580). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Of Tennessee, 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

Metaxalone 800mg #30 (Metaxalone 800mg 80425 0580 01)

Label for Metaxalone 800 mg tablet, quantity of 30, from Advanced Rx of Tennessee, LLC. The label includes storage instructions, barcode, NDC number 80425-0580-01, and expiration date 12/31/2030. It also references comparison to SKELAXIN and states 'Rx Only.'*

FDA Label Image

Metaxalone 800mg #60 (Metaxalone 800mg 80425 0580 02)

Label for Metaxalone 800 mg tablet, quantity of 60, from Advanced Rx of Tennessee, LLC, Nashville, TN. Includes NDC 80425-0580-02 and batch information with expiration date 12/31/2030. The label notes comparison to Skelaxin and provides storage instructions between 20° and 25°C (68° and 77°F).*

FDA Label Image

Metaxalone 800mg #90 (Metaxalone 800mg 80425 0580 03)

Label for Metaxalone 800 mg oral tablets, quantity of 90 tablets. The label indicates the labeler as Advanced Rx of Tennessee, LLC, with storage instructions between 20°C and 25°C (68°F to 77°F). Includes a barcode, lot number placeholder, and expiration date placeholder of 12/31/2030. The label states the product is prescription only and compared to Skelaxin, with the NDC 80425-0580-03.*

FDA Label Image

Image (Metaxalone Tablets 1)

Chemical structure of Metaxalone, showing its molecular framework including a dimethyl-substituted aromatic ring connected via an ether linkage to a morpholine-2-one moiety.*

* 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.