Nabumetone 750 Mg
Product Images NDC 0722-7077

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Nabumetone 750 Mg (NDC 0722-7077). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nexgen Pharma, 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

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

Chemical structure of nabumetone, the active ingredient in Nabumetone 750 mg by Nexgen Pharma, Inc. The structure shows a methoxy-substituted naphthalene ring with a carboxylic acid functional group.*

FDA Label Image

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

A line chart depicting concentration over time in hours for four dosage conditions of 1000 mg and 2000 mg doses, showing mean values with standard deviations (±2 SD). The graph illustrates concentration decline over a 70-hour period with two dosage labels indicated at 1000 mg/day and 2000 mg/day.*

FDA Label Image

Structural Formula (Nabumetone)

Chemical structure diagram of the active ingredient in Nabumetone 750 mg, showing the molecular arrangement with labeled functional groups consistent with nabumetone's chemical composition.*

FDA Label Image

1000mg 30 Tablets Container Label (Image 02)

Nabumetone 1000 mg Tablets USP label from Nexgen Pharma, Inc. The label shows active ingredient nabumetone USP 1000 mg per tablet, package size of 30 tablets, and storage instructions at controlled room temperature. It includes the NDC number 0722-7078-30 and a barcode.*

FDA Label Image

500mg 500 Tablets Container Label (Seialized 7076 Nabumetone 500 mg 500s)

Nabumetone Tablets USP 500 mg label from Nexgen Pharma, Inc. The label states each tablet contains 500 mg nabumetone. It includes storage instructions at controlled room temperature and advises pharmacists to dispense with a medication guide. The package size is 500 tablets.*

FDA Label Image

500mg 100 Tablets Container Label (Serialized 7076 Nabumetone 500 mg 100s)

Label for Nabumetone Tablets USP 500 mg, manufactured by Nexgen Pharma, Inc. The label includes the NDC code 0722-7076-01, specifies each tablet contains 500 mg nabumetone, and states a 100 tablet count. It advises dispensing with a medication guide and storing between 20° to 25°C (68° to 77°F).*

FDA Label Image

750mg 100 Tablets Container Label (Serialized 7077 Nabumetone 750 mg 100s)

Nabumetone Tablets USP 750 mg label indicating each tablet contains 750 mg nabumetone. The label includes manufacturer Nexgen Pharma, Inc., storage instructions, a barcode, and states the package contains 100 tablets for prescription use.*

FDA Label Image

750mg 500 Tablets Container Label (Serialized 7077 Nabumetone 750 mg 500s)

Nabumetone Tablets USP 750 mg label from Nexgen Pharma, Inc. The label indicates each tablet contains 750 mg of nabumetone and includes instructions for pharmacists to dispense with a medication guide separately. It states storage temperature, child-resistant packaging instructions, and that it is Rx only with 500 tablets per container. The label also features a barcode and manufacturer address in Irvine, CA.*

FDA Label Image

1000mg 100 Tablets Container Label (Serialized 7078 Nabumetone 1000 mg 100s)

Label of Nabumetone Tablets USP 1000 mg manufactured by Nexgen Pharma, Inc. The label includes the NDC 0722-7078-01 and specifies each tablet contains nabumetone USP 1000 mg. Packaging indicates 100 tablets per container and includes storage and dispensing instructions.*

* 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.