Nabumetone Tablet
Product Images NDC 51655-733

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nabumetone (NDC 51655-733). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, 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

FDA Label Image

Label (51655 733 52 Master Bottle Label Approval Rev A 07 21)

Label (51655 733 52 Master Bottle Label Approval Rev A 07 21)
Nabumetone 750 mg Tablets, USP, oral tablet dosage form. The label indicates a package of 30 tablets for prescription use only. The label shows storage instructions and is from Northwind Health Company, LLC, including NDC 51655-733-52.*
FDA Label Image

Figure1 (Figure1)

Figure1 (Figure1)
A line graph showing plasma concentrations of Nabumetone active metabolite (6MNA) over 70 hours. The graph compares steady-state concentrations after once-daily dosing of 1000 mg and 2000 mg Nabumetone, including standard deviation ranges for each dose. Concentration is measured in ng/mL on the Y-axis, and time in hours on the X-axis.*
FDA Label Image

Structure1 (Structure1)

Structure1 (Structure1)
Chemical structure of nabumetone displayed with molecular formula C15H16O2 and molecular weight 228.3.*
FDA Label Image

Structure2 (Structure2)

Structure2 (Structure2)
Chemical structure diagram of 6-methoxy-2-naphthylacetic acid (6MNA), an active metabolite of Nabumetone, showing aromatic rings, methoxy group, and carboxylic acid functional group.*

* 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.