Nabumetone Tablet
Product Images NDC 72162-1557

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 72162-1557). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Figure1 (Figure1)

Figure1 (Figure1)
A line graph showing Nabumetone active metabolite (6MNA) plasma concentrations over 70 hours at steady state following once-daily dosing of 1000 mg (n=31) and 2000 mg (n=12). The graph displays concentration ranges with ±2 standard deviations for both dosage levels, illustrating how plasma concentration decreases over time.*
FDA Label Image

Label (Lbl721621557)

Label (Lbl721621557)
Nabumetone Tablets, USP 500 mg oral tablets label. The label shows the NDC 72162-1557-1, contains 100 tablets, and is relabeled by Bryant Ranch Prepack, Inc., Burbank, CA, with manufacturing by ScieGen Pharmaceuticals, Inc. Storage and handling instructions are also included.*
FDA Label Image

Structure1 (Structure1)

Structure1 (Structure1)
Chemical structure of Nabumetone showing its molecular formula (C15H16O2) and molecular weight (228.3). The structure includes a naphthalene ring with a methoxy group and a ketone side chain.*
FDA Label Image

Structure2 (Structure2)

Structure2 (Structure2)
Chemical structure diagram of 6-methoxy-2-naphthylacetic acid (6MNA), the active metabolite of Nabumetone. The diagram shows ring structures, 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.