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  5. NDC Package Code: 14445-156-05 Febuxostat

NDC Package 14445-156-05 Febuxostat

View Billable Units, 11-Digit Format, RxNorm

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.

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:
14445-156-05
Package Description:
500 TABLET, FILM COATED in 1 BOTTLE
Product Code:
14445-156
Proprietary Name:
Febuxostat
Usage Information:
Febuxostat is used to lower uric acid levels in people with gout. Febuxostat works by reducing the amount of uric acid made by the body. An increased uric acid level can cause gout. Because of the risk of very serious heart-related problems and stroke with febuxostat (see also Warning section), febuxostat should be used only after treatment with a medication called allopurinol did not work to lower your uric acid level, caused serious side effects, or is not recommended by your doctor. Febuxostat should be used only if you have symptoms caused by a high blood uric acid level.
11-Digit NDC Billing Format:
14445015605
NDC to RxNorm Crosswalk:
Labeler Name:
Indoco Remedies Limited
Sample Package:
No
FDA Application Number:
ANDA210292
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
02-14-2017
Listing Expiration Date:
12-31-2024
Exclude Flag:
I
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
14445-156-3030 TABLET, FILM COATED in 1 BOTTLE
14445-156-9090 TABLET, FILM COATED in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 14445-156-05?

The NDC Packaged Code 14445-156-05 is assigned to a package of 500 tablet, film coated in 1 bottle of Febuxostat, labeled by Indoco Remedies Limited. The product's dosage form is and is administered via form.

Is NDC 14445-156 included in the NDC Directory?

No, Febuxostat with product code 14445-156 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Indoco Remedies Limited on February 14, 2017 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 14445-156-05?

The 11-digit format is 14445015605. 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
5-3-214445-156-055-4-214445-0156-05