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  5. NDC Package Code: 51655-396-25 Nabumetone

NDC Package 51655-396-25 Nabumetone

Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
51655-396-25
Package Description:
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Code:
51655-396
Proprietary Name:
Nabumetone
Non-Proprietary Name:
Nabumetone
Substance Name:
Nabumetone
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.
11-Digit NDC Billing Format:
51655039625
NDC to RxNorm Crosswalk:
  • RxCUI: 311892 - nabumetone 500 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Northwind Pharmaceuticals, Llc
    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(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • NABUMETONE 500 mg/1
    • Pharmacologic Class(es):
  • Anti-Inflammatory Agents, Non-Steroidal - [CS]
  • Cyclooxygenase Inhibitors - [MoA] (Mechanism of Action)
  • Nonsteroidal Anti-inflammatory Drug - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA078671
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-07-2020
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Frequently Asked Questions

    What is NDC 51655-396-25?

    The NDC Packaged Code 51655-396-25 is assigned to a package of 60 tablet, film coated in 1 bottle, plastic of Nabumetone, a human prescription drug labeled by Northwind Pharmaceuticals, Llc. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 51655-396 included in the NDC Directory?

    Yes, Nabumetone with product code 51655-396 is active and included in the NDC Directory. The product was first marketed by Northwind Pharmaceuticals, Llc on July 07, 2020 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 51655-396-25?

    The 11-digit format is 51655039625. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-251655-396-255-4-251655-0396-25