Nabumetone Tablet
Product Images NDC 55700-840

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 55700-840). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Quality Care Products, 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

1

1
Label for Nabumetone 750 mg tablets showing a bottle or carton label with proprietary and generic name Nabumetone, strength 750 mg, and quantity of 60 tablets. The label notes the product is for oral use, Rx only, and each tablet contains Nabumetone. It is packaged and distributed by Quality Care Products, LLC in Holland, OH, with manufacturing by ScieGen Pharmaceuticals, Inc. The label includes storage instructions (68 to 77 degrees F), GTIN, NDC 55700-840-60, and a barcode.*
FDA Label Image

Figure1 (Figure1)

Figure1 (Figure1)
A pharmacokinetic chart showing Nabumetone active metabolite (6MNA) plasma concentrations over 70 hours at steady state following once-daily dosing of Nabumetone at 1000 mg and 2000 mg doses. The y-axis shows concentration in ng/mL, and the x-axis shows time in hours, with shaded areas representing ±2 standard deviations for each dose group.*
FDA Label Image

Structure1 (Structure1)

Structure1 (Structure1)
Chemical structure of Nabumetone showing its molecular arrangement with a methoxy-substituted naphthalene ring linked to a ketone group via a butyl chain.*
FDA Label Image

Structure2 (Structure2)

Structure2 (Structure2)
Chemical structure of Nabumetone, showing its molecular arrangement including a methoxy group on a naphthalene ring and a carboxylic acid 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.