Nabumetone Tablet
Product Images NDC 55700-845

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 55700-845). 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

Image Description (New Doc 2020 03 02 09.49.10 1)

Image Description (New Doc 2020 03 02 09.49.10 1)
Label for Nabumetone 500 mg tablets by Quality Care Products, LLC. The label indicates 30 white, oval tablets with NDC 55700-0845-30. Manufactured by ScieGen Pharmaceuticals, Inc., Hauppauge, NY. It includes storage and safety warnings and contact information.*
FDA Label Image

Figure1 (Figure1)

Figure1 (Figure1)
A pharmacokinetic graph showing Nabumetone active metabolite (6MNA) plasma concentrations over 70 hours at steady state following once-daily dosing of 1000 mg and 2000 mg. The chart includes mean concentration curves and ±2 standard deviation ranges for both doses, with plasma concentration (ng/mL) on Y-axis and time (hours) on X-axis.*
FDA Label Image

Structure1 (Structure1)

Structure1 (Structure1)
Chemical structure of nabumetone, showing its molecular framework with rings and functional groups forming the active ingredient of the Nabumetone 500 mg oral tablet by Quality Care Products, LLC.*
FDA Label Image

Structure2 (Structure2)

Structure2 (Structure2)
Chemical structure of nabumetone, showing the arrangement of its aromatic rings and functional groups including a methoxy and a carboxyl 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.