Nabumetone
Product Images NDC 10544-120

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nabumetone (NDC 10544-120). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Blenheim Pharmacal, 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

Image Description (Label Nabumetone Tabs 500mg Bpi(10544 120 20) Watson(0591 3670 05) Rev1)

Nabumetone Tablets USP 500mg carton label showing a package of 20 tablets. The label includes the proprietary name, strength, dosage form, prescription-only status, storage instructions, and manufacturer information identifying Blenheim Pharmacal, Inc. The NDC 10544-120-20 and manufacturing code are also present along with barcodes.*

FDA Label Image

Structure (Nabumetone 1)

Chemical structure of Nabumetone is shown as a molecular diagram depicting its bonds and atoms. The image also includes its molecular formula C15H16O2 and molecular weight 228.29.*

FDA Label Image

6mna (Nabumetone 2)

Chemical structure of Nabumetone showing a methoxy group attached to a naphthalene ring and a carboxyl group. The structure depicts the key molecular features of the active ingredient Nabumetone.*

FDA Label Image

Figure (Nabumetone 3)

A concentration versus time graph showing plasma levels of Nabumetone over about 70 hours. The plot includes shaded regions and lines representing ±2 standard deviations for 1000 mg and 2000 mg daily doses. Concentration is measured in mcg/mL on the vertical axis, and time in hours on the horizontal axis. Arrows mark 1000 mg/day and 2000 mg/day dose points around 48 hours.*

* 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.