Nabumetone Tablet
Product Images NDC 60760-368

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nabumetone (NDC 60760-368). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by St. Mary's Medical Park Pharmacy, 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

Nab (Nabumetone 60760 368 15)

Nabumetone Tablets USP 500 mg oral tablets packaging label showing NDC 60760-368-15. The label includes quantity 15, placeholder lot number, and expiration date. Manufactured by ScieGen Pharmaceuticals, Inc. and packaged by St. Mary's Medical Park Pharmacy in Oro Valley, AZ. Storage instructions specify controlled room temperature 15°-30°C (59°-86°F). Rx only label is present.*

FDA Label Image

Figure1 (Figure1)

A line graph showing Nabumetone active metabolite (6MNA) plasma concentrations over 70 hours at steady state after once-daily dosing of Nabumetone at 1000 mg and 2000 mg. The graph includes mean concentrations and standard deviations (+2 SD and -2 SD) for both dosages, with concentrations on the y-axis (mg/mL) and time on the x-axis (hours).*

FDA Label Image

Structure1 (Structure1)

Chemical structure of Nabumetone, a human prescription drug. The diagram depicts the molecular structure including its aromatic rings and functional groups, representing the active ingredient Nabumetone.*

FDA Label Image

Structure2 (Structure2)

Chemical structure of nabumetone displayed as a two-ring system with a carboxylic acid group and a methoxy substituent.*

* 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.