Nabumetone 500 Mg Tablet, Film Coated
NDC Package 79739-7076-5

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Nabumetone 500 Mg (nabumetone) tablets is nabumetone is used to reduce pain, swelling, and joint stiffness from arthritis. This formulation utilizes a tablet, film coated delivery system. Marketed by Lgm Pharma Solutions, Llc, this product is identified by NDC 79739-7076 and is authorized under FDA application ANDA203166.

Identification & Billing

NDC Package Code
79739-7076-5
Package Description
500 TABLET, FILM COATED in 1 BOTTLE
Product Code
11-Digit Billing Format
79739707605
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Nabumetone 500 Mg
Non-Proprietary Name
Nabumetone
Substance Name
Nabumetone
Dosage Form
Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Usage Information
Nabumetone is used to reduce pain, swelling, and joint stiffness from arthritis. This medication is known as a nonsteroidal anti-inflammatory drug (NSAID). If you are treating a chronic condition such as arthritis, ask your doctor about non-drug treatments and/or using other medications to treat your pain. See also Warning section.

Regulatory & Marketing

Labeler Name
Lgm Pharma Solutions, Llc
Product Type
Human Prescription Drug
FDA Application #
ANDA203166
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
09-04-2019
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (79739-7076). Click a package code to view its specific billing and regulatory data.

100 TABLET, FILM COATED in 1 BOTTLE

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 79739-7076-5 identifies a specific commercial package of 500 tablet, film coated in 1 bottle of Nabumetone 500 Mg, a human prescription drug labeled by Lgm Pharma Solutions, Llc. This tablet, film coated is formulated for oral use and contains nabumetone as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Lgm Pharma Solutions, Llc on September 04, 2019. The current certification is valid through December 31, 2026.

What are the primary indications for this medication?

Nabumetone is used to reduce pain, swelling, and joint stiffness from arthritis. This medication is known as a nonsteroidal anti-inflammatory drug (NSAID). If you are treating a chronic condition such as arthritis, ask your doctor about non-drug treatments and/or using other medications to treat your pain. See also Warning section.

How is this Lgm Pharma Solutions, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 79739707605. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
79739-7076-5
11-Digit CMS (5-4-2)
79739-7076-05

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.