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  5. NDC Package Code: 16714-841-01 Dofetilide

NDC Package 16714-841-01 Dofetilide

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 discontinued by the firm.

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:
16714-841-01
Package Description:
60 CAPSULE in 1 BOTTLE, PLASTIC
Product Code:
16714-841
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:
16714084101
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
60 EA
Labeler Name:
Northstar Rx Llc
Sample Package:
No
FDA Application Number:
ANDA207058
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
06-18-2018
End Marketing Date:
06-30-2024
Listing Expiration Date:
06-30-2024
Exclude Flag:
D
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 16714-841-01?

The NDC Packaged Code 16714-841-01 is assigned to a package of 60 capsule in 1 bottle, plastic of Dofetilide, labeled by Northstar Rx Llc. The product's dosage form is and is administered via form.

Is NDC 16714-841 included in the NDC Directory?

No, Dofetilide with product code 16714-841 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Northstar Rx Llc on June 18, 2018 and its listing in the NDC Directory is set to expire on June 30, 2024 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 16714-841-01?

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 16714-841-01?

The 11-digit format is 16714084101. 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
5-3-216714-841-015-4-216714-0841-01