1. Home
  2. Labeler Index
  3. Tya Pharmaceuticals
  4. 64725-1324
  5. NDC Package Code: 64725-1324-1 Digox

NDC Package 64725-1324-1 Digox

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
64725-1324-1
Package Description:
100 TABLET in 1 BOTTLE
Product Code:
64725-1324
Proprietary Name:
Digox
Usage Information:
Digoxin is used to treat heart failure, usually along with other medications. It is also used to treat certain types of irregular heartbeat (such as chronic atrial fibrillation). Treating heart failure may help maintain your ability to walk and exercise and may improve the strength of your heart. Treating an irregular heartbeat can also improve your ability to exercise. Digoxin belongs to a class of medications called cardiac glycosides. It works by affecting certain minerals (sodium and potassium) inside heart cells. This reduces strain on the heart and helps it maintain a normal, steady, and strong heartbeat.
11-Digit NDC Billing Format:
64725132401
NDC to RxNorm Crosswalk:
  • RxCUI: 1245443 - Digox 125 MCG Oral Tablet
  • RxCUI: 1245443 - digoxin 0.125 MG Oral Tablet [Digox]
  • RxCUI: 1245443 - Digox 0.125 MG Oral Tablet
  • RxCUI: 197604 - digoxin 125 MCG Oral Tablet
  • RxCUI: 197604 - digoxin 0.125 MG Oral Tablet
    • Labeler Name:
    Tya Pharmaceuticals
    Sample Package:
    No
    Start Marketing Date:
    07-26-2002
    Listing Expiration Date:
    12-31-2017
    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.

    Frequently Asked Questions

    What is NDC 64725-1324-1?

    The NDC Packaged Code 64725-1324-1 is assigned to a package of 100 tablet in 1 bottle of Digox, labeled by Tya Pharmaceuticals. The product's dosage form is and is administered via form.

    Is NDC 64725-1324 included in the NDC Directory?

    No, Digox with product code 64725-1324 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Tya Pharmaceuticals on July 26, 2002 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 64725-1324-1?

    The 11-digit format is 64725132401. 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 5-4-1 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
    5-4-164725-1324-15-4-264725-1324-01