Nabumetone Tablet
Product Images NDC 72789-040

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nabumetone (NDC 72789-040). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx 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

72789040 Label (72789040)

Label for Nabumetone USP 750 mg oral tablets, containing 30 tablets per package. The label shows the NDC 72789-040-30 and is manufactured by PD-Rx Pharmaceuticals, Inc., Oklahoma City, OK. It includes dosage form, strength, package count, reorder number, lot number C22B93, and expiration date 10/2023. Additional warnings and usage instructions appear on the label.*

FDA Label Image

Figure1 (Figure1)

A graph showing Nabumetone active metabolite (6MNA) plasma concentrations over time at steady state following once-daily dosing of Nabumetone at 1000 mg and 2000 mg doses. The y-axis represents concentration in mg/mL and the x-axis represents time in hours. The graph includes shaded areas illustrating the concentration ranges with minus and plus two standard deviations for both 1000 mg and 2000 mg doses.*

FDA Label Image

Structure1 (Structure1)

Chemical structure of nabumetone showing a fused bicyclic ring system with a methoxy group and a ketone functional group at the end of a carbon chain. The molecular formula is C15H16O2 with a molecular weight of 228.3.*

FDA Label Image

Structure2 (Structure2)

Chemical structure of 6-methoxy-2-naphthylacetic acid (6MNA), a metabolite of Nabumetone, showing a naphthalene ring with a methoxy group and an acetic acid side chain.*

* 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.