Nabumetone 500 Mg Tablet, Film Coated
Product Images NDC 79739-7076

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Nabumetone 500 Mg (NDC 79739-7076). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lgm Pharma Solutions, Llc, 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

6mna Structural Formula (6 Methoxy 2 Naphthylacetic Acid (6mna))

Chemical structure of nabumetone, depicting its molecular framework including aromatic rings, a methoxy group, and a carboxylic acid functional group.*

FDA Label Image

Nabumetone Active Metabolite Plasma Concentrations (6adc50d6 C4a2 4bc7 85f8 61f281f632fc 02)

A shaded area plot showing concentration versus time over 70 hours for Nabumetone at dosages of 1000 mg and 2000 mg per day. The graph includes mean concentration curves and shaded regions representing ±2 standard deviations around the mean for each dosage. Concentrations peak early and decline over time for both dosages.*

FDA Label Image

Structural Formula (Nabumetone)

Chemical structure diagram of nabumetone, showing its molecular framework including a naphthalene ring with a methoxy group and a ketone functional group attached to an aliphatic side chain.*

FDA Label Image

Nabumetone (1000 mg)

Label for Nabumetone Tablets USP 1000 mg film-coated oral tablets by LGM Pharma Solutions, LLC. The label includes dosage strength, directions to dispense with a medication guide, storage instructions, and a barcode. The package contains 30 tablets and is for prescription use only.*

FDA Label Image

Nabumetone (500 mg)

Nabumetone 500 mg tablets USP label from LGM Pharma Solutions, LLC. The label indicates 500 tablets in the package with the active ingredient nabumetone 500 mg per tablet. It includes storage instructions, pharmacist dispensing information, and a barcode. The label also displays NDC 79739-7076-5 and manufacturer details.*

FDA Label Image

Nabumetone (500 mg)

The label is for Nabumetone Tablets USP, 500 mg, a prescription oral film-coated tablet by LGM Pharma Solutions, LLC. It includes the NDC 79739-7076-1 and specifies each tablet contains 500 mg nabumetone. The label advises dispensing with a medication guide and storing at controlled room temperature. Package count is 100 tablets.*

FDA Label Image

Nabumetone (750 mg)

Label for Nabumetone Tablets USP 750 mg, film-coated tablets for oral use. The label includes the active ingredient name and strength, an NDC number (79739-7077-1), dosage instructions to see the package insert, storage conditions, and a warning to keep out of reach of children. It states the product contains 100 tablets and is manufactured by LGM Pharma Solutions, LLC in Irvine, CA. The label also features a barcode and a QR code for identification.*

FDA Label Image

Nabumetone (750 mg)

Nabumetone Tablets USP 750 mg film-coated oral tablets label shows each tablet contains 750 mg nabumetone. The label includes dispensing instructions, storage conditions, and manufacturer details for LGM Pharma Solutions, LLC. It features the NDC 79739-7077-5, a barcode, and states the package contains 500 tablets.*

FDA Label Image

Nabumetone (1000 mg)

Nabumetone 1000 mg Tablets USP film-coated oral tablets label from LGM Pharma Solutions, LLC. The label includes dosage strength, pharmacist dispensing instructions, storage conditions, manufacturer information, a barcode, and states the package contains 100 tablets. It specifies prescription use only and child-resistant container requirements.*

* 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.