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  5. NDC Package Code: 63739-510-10 Propafenone Hcl

NDC Package 63739-510-10 Propafenone Hcl

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:
63739-510-10
Package Description:
10 BLISTER PACK in 1 BOX, UNIT-DOSE / 10 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
63739-510
Proprietary Name:
Propafenone Hcl
Usage Information:
This medication is used to treat certain types of serious (possibly fatal) irregular heartbeat (such as paroxysmal supraventricular tachycardia and atrial fibrillation). It is used to restore normal heart rhythm and maintain a regular, steady heartbeat. Propafenone 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:
63739051010
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
10 EA
Labeler Name:
Mckesson Corporation Dba Sky Packaging
Sample Package:
No
FDA Application Number:
ANDA075203
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
10-24-2000
End Marketing Date:
03-31-2015
Listing Expiration Date:
03-31-2015
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 63739-510-10?

The NDC Packaged Code 63739-510-10 is assigned to a package of 10 blister pack in 1 box, unit-dose / 10 tablet, film coated in 1 blister pack of Propafenone Hcl, labeled by Mckesson Corporation Dba Sky Packaging. The product's dosage form is and is administered via form.

Is NDC 63739-510 included in the NDC Directory?

No, Propafenone Hcl with product code 63739-510 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Mckesson Corporation Dba Sky Packaging on October 24, 2000 and its listing in the NDC Directory is set to expire on March 31, 2015 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 63739-510-10?

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 10.

What is the 11-digit format for NDC 63739-510-10?

The 11-digit format is 63739051010. 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
5-3-263739-510-105-4-263739-0510-10