1 (Metaxalone Tablets 1)
Metaxalone Tablet
Product Images NDC 65162-553
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Product Visual Gallery
This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metaxalone (NDC 65162-553). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Amneal Pharmaceuticals 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.
Product Images & Figures Index
1 (Metaxalone Tablets 2)
This is a graph representing the concentration (in nanograms per milliliter) of Metaxalone following ingestion of an 800 milligram dose under fasted and fed conditions. The x-axis shows the time in hours and the y-axis displays the concentration values. The graph demonstrates that the concentration of Metaxalone is higher when taken under fed conditions, peaking at around 5,000 ng/mL after 4 hours, as opposed to around 2,000 ng/mL after 2 hours under fasted conditions.*
1 (Metaxalone Tablets 3)
This is a description of a medicine with the National Drug Code (NDC) of 65162-553-10. The medicine is identified as MetaJp(aIone Tablets, USP, containing 800mg of Metaxalone, which is recommended for use in adults and children over 12 years old at a dose of one tablet (800 mg) three to four times a day. The pack contains 100 tablets and is sealed for protection. The container should be stored between 20-25°C (68-77°F) and excursions are allowed between 15-30°C (59-86°F) [see USP Controlled Room Temperature]. The medicine should be dispensed in a well-closed container. The manufacturer is Amneal Pharmaceuticals Pvt. Ltd. in Ahmedabad, India, and the product is distributed by Amneal Pharmaceuticals LLC in Bridgewater, NJ. No additional information is provided.*
* 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.
