Nabumetone
NDC Package 63874-607-90

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Nabumetone is used to reduce pain, swelling, and joint stiffness from arthritis. Marketed by Altura Pharmaceuticals, Inc., this product is identified by NDC 63874-607 and is authorized under FDA application ANDA076009.

Identification & Billing

NDC Package Code
63874-607-90
Package Description
90 TABLET in 1 BOTTLE, PLASTIC
Product Code
63874-607
11-Digit Billing Format
63874060790
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Nabumetone
Dosage Form
-
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
Altura Pharmaceuticals, Inc.
FDA Application #
ANDA076009
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
01-01-2010
Listing Expiration
12-31-2017
Exclude Flag
I
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 (63874-607). Click a package code to view its specific billing and regulatory data.

63874-607-01
100 TABLET in 1 BOTTLE, PLASTIC
63874-607-30
30 TABLET in 1 BOTTLE, PLASTIC
63874-607-60
60 TABLET in 1 BOTTLE, PLASTIC

* 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 63874-607-90 identifies a specific commercial package of 90 tablet in 1 bottle, plastic of Nabumetone, labeled by Altura Pharmaceuticals, Inc.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Altura Pharmaceuticals, Inc. on January 01, 2010. The current certification is valid through December 31, 2017.

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 Altura Pharmaceuticals, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 63874060790. 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 (5-3-2)
63874-607-90
11-Digit CMS (5-4-2)
63874-0607-90

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