Nabumetone Tablet
Product Images NDC 68788-7765

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nabumetone (NDC 68788-7765). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Preferred Pharmaceuticals, 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

Nabumetone Tablet Usp 500mg (Container1)

Nabumetone Tab USP 500mg oral tablet label from Preferred Pharmaceuticals, Inc. The label states each tablet contains Nabumetone USP 500mg. It includes storage instructions, manufacturer info for ScieGen Pharmaceuticals, Inc., and caution about federal law regarding drug transfer. Directions are provided in both English and Spanish on a yellow background with blanks for dosage details. Barcodes and product identification fields are also present.*

FDA Label Image

Figure1 (Figure1)

A line chart showing Nabumetone active metabolite (6MNA) plasma concentrations over time at steady state following once-daily dosing of Nabumetone at 1000 mg and 2000 mg. The y-axis represents concentration in mcg/mL, and the x-axis represents time in hours. The chart includes curves with standard deviation ranges for both dosage levels, demonstrating plasma concentration decline over 70 hours.*

FDA Label Image

Structure1 (Structure1)

Chemical structure of the active ingredient Nabumetone, showing its molecular formula C15H16O2 and molecular weight of 228.3.*

FDA Label Image

Structure2 (Structure2)

Chemical structure of 6-methoxy-2-naphthylacetic acid (6MNA), the active metabolite of Nabumetone, showing a naphthalene ring with methoxy and acetic acid functional groups.*

* 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.