Nabumetone Tablet, Film Coated
Product Images NDC 70954-785

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Nabumetone (NDC 70954-785). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ani Pharmaceuticals, 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

Figure-1 (Figure 1)

A line graph showing Nabumetone active metabolite (6MNA) plasma concentrations over time at steady state after once-daily dosing of 1000 mg and 2000 mg. The x-axis represents time in hours (0 to 70), and the y-axis shows concentration in ng/mL (0 to 120). The graph includes mean concentrations with plus and minus two standard deviations for both dose levels.*

FDA Label Image

Label-1 (Label 1)

Label for Nabumetone Tablets, USP 500 mg film-coated tablets by ANI Pharmaceuticals, Inc. The label indicates 100 tablets per container, prescription only, with storage instructions and a barcode. The distributing company information and issuance date of 06/2024 are also shown.*

FDA Label Image

Label-2 (Label 2)

Label for Nabumetone Tablets USP, 500 mg, film-coated oral tablets. The label specifies dispensing a medication guide to each patient and includes storage instructions for controlled room temperature. Distributed by ANI Pharmaceuticals, Inc., the label shows an Rx only designation for 500 tablets in the package along with a barcode and lot/expiry placeholders.*

FDA Label Image

Label-3 (Label 3)

Nabumetone Tablets USP 750 mg, film-coated oral tablets in a package of 100 tablets. The label includes dispensing and storage instructions, a barcode, and the distributor Ani Pharmaceuticals, Inc. The label specifies prescription-only use and advises dispensing the medication guide to patients.*

FDA Label Image

Label-4 (Label 4)

Nabumetone Tablets USP 750 mg film-coated tablet label from ANI Pharmaceuticals, Inc. The label specifies 500 tablets per container and includes storage instructions, barcode, lot number, expiration date, and medication guide warning.*

FDA Label Image

Structure-2 (Structure 2)

Chemical structure of the active ingredient Nabumetone, showing a methoxy-substituted naphthalene ring with a propionic acid side chain.*

FDA Label Image

Structure (Structure)

Chemical structure of Nabumetone, showing its molecular formula C15H16O2 and molecular weight of 228.3. The diagram depicts the arrangement of carbon, hydrogen, and oxygen atoms specific to Nabumetone.*

* 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.