Nabumetone Tablet
Product Images NDC 70518-4047

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 70518-4047). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Nabumetone 750 mg tablet label showing a quantity of 14 tablets. The label includes the NDC number 70518-4047-00 and indicates the product is for prescription use only. The labeler is RemedyRepack Inc., with manufacturing by ScieGen Pharmaceuticals, Inc. Storage instructions specify 20-25°C with permitted excursions. A barcode and QR code are also visible.*
FDA Label Image

Figure1 (Figure1)

Figure1 (Figure1)
A line graph showing Nabumetone active metabolite (6MNA) plasma concentrations over time at steady state following once-daily dosing of Nabumetone at 1000 mg (n=31) and 2000 mg (n=12). The y-axis represents concentration in mg/mL, and the x-axis represents time in hours. The plot includes shaded areas indicating ±2 standard deviations for each dose.*
FDA Label Image

Structure1 (Structure1)

Structure1 (Structure1)
Chemical structure of Nabumetone, showing the molecular formula C15H16O2 and a molecular weight of 228.3. The diagram displays the arrangement of atoms and bonds in the compound's structure.*
FDA Label Image

Structure2 (Structure2)

Structure2 (Structure2)
Chemical structure of 6-methoxy-2-naphthylacetic acid (6MNA), the active metabolite of Nabumetone, shown with aromatic rings, 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.