NDC Package 51862-025-60 Dofetilide

View Billable Units, 11-Digit Format, RxNorm

Package Information
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:

51862-025-60

Package Description:

60 CAPSULE in 1 BOTTLE, PLASTIC

Product Code:

51862-025

Proprietary Name:

Dofetilide

Usage Information:

This medication is used to treat certain types of serious (possibly fatal) irregular heartbeat (such as atrial fibrillation/flutter). It is used to restore normal heart rhythm and maintain a regular, steady heartbeat. Dofetilide is known as an anti-arrhythmic drug. It works by blocking the activity of certain electrical signals in the heart that can cause an irregular heartbeat. Treating an irregular heartbeat can decrease the risk for blood clots, and this effect can reduce your risk of heart attack or stroke.

11-Digit NDC Billing Format:

51862002560

Billing Unit:

EA - Billing unit of "each" is used when the product is dispensed in discreet units.

NDC to RxNorm Crosswalk:

60 EA

NDC to RxNorm Crosswalk:

RxCUI: 310003 - dofetilide 125 MCG Oral Capsule

RxCUI: 310003 - dofetilide 0.125 MG Oral Capsule

RxCUI: 310004 - dofetilide 250 MCG Oral Capsule

RxCUI: 310004 - dofetilide 0.25 MG Oral Capsule

RxCUI: 310005 - dofetilide 500 MCG Oral Capsule

Labeler Name:

Mayne Pharma Inc.

Sample Package:

Start Marketing Date:

06-07-2016

Listing Expiration Date:

12-31-2023

Exclude Flag:

Code Structure:

51862 - Mayne Pharma Inc.
- 51862-025 - Dofetilide
  - 51862-025-60 - 60 CAPSULE in 1 BOTTLE, PLASTIC

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 51862-025-60?

The NDC Packaged Code 51862-025-60 is assigned to a package of 60 capsule in 1 bottle, plastic of Dofetilide, labeled by Mayne Pharma Inc.. The product's dosage form is and is administered via form.

Is NDC 51862-025 included in the NDC Directory?

No, Dofetilide with product code 51862-025 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Mayne Pharma Inc. on June 07, 2016 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 51862-025-60?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 60.

What is the 11-digit format for NDC 51862-025-60?

The 11-digit format is 51862002560. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	51862-025-60	5-4-2	51862-0025-60

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