Nabumetone Tablet
Product Images NDC 71335-2292

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 71335-2292). 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.

FDA Label Image

Figure1 (Figure1)

Figure1 (Figure1)
A line chart depicting Nabumetone active metabolite (6MNA) plasma concentrations over 70 hours at steady state following once-daily dosing of 1000 mg and 2000 mg. The graph includes standard deviation ranges for both doses, showing concentration decline over time with labeled daily doses at around 44 hours.*
FDA Label Image

Label (Lbl713352292)

Label (Lbl713352292)
Label for Nabumetone Tablets USP 500 mg, 500 count, repackaged by Bryant Ranch Prepack and manufactured by ScieGen Pharmaceuticals, Inc. The label includes storage instructions, child-resistant container notice, and a link to the medication guide, with both 2D and linear barcodes and the NDC 71335-2292-1.*
FDA Label Image

Structure1 (Structure1)

Structure1 (Structure1)
Chemical structure of Nabumetone showing a naphthalene derivative with a methoxy group and a ketone side chain. The molecular formula C15H16O2 and molecular weight 228.3 are indicated below the structure.*
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 aromatic rings with methoxy and carboxylic acid functional groups.*

* 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.