Nabumetone Tablet
Product Images NDC 51655-446

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 51655-446). 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.

FDA Label Image

Label (51655 446 20 Master Bottle Label Approval Rev A 10 20)

Label (51655 446 20 Master Bottle Label Approval   Rev A 10 20)
Label for Nabumetone Tablets USP 500 mg, containing 20 tablets for oral use. The label includes storage instructions, caution for Rx only, and manufacturer details for Northwind Health Company, LLC. The NDC is 51655-446-20.*
FDA Label Image

Figure1 (Figure1)

Figure1 (Figure1)
A line graph showing plasma concentrations of Nabumetone's active metabolite (6MNA) over time after once-daily dosing at 1000 mg and 2000 mg. The x-axis represents time in hours, and the y-axis shows concentration in mcg/mL. Shaded areas depict concentration ranges with standard deviations for both dose levels.*
FDA Label Image

Structure1 (Structure1)

Structure1 (Structure1)
Chemical structure diagram of Nabumetone displaying its molecular formula (C15H16O2) and molecular weight (228.3). The structure includes rings, a methoxy group, and a ketone functional group, consistent with the active ingredient Nabumetone.*
FDA Label Image

Structure2 (Structure2)

Structure2 (Structure2)
Chemical structure of 6-methoxy-2-naphthylacetic acid (6MNA), the active metabolite of Nabumetone, showing its molecular layout with a methoxy group, naphthalene ring, 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.