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  5. NDC Package Code: 70515-115-06 Betapace Af

NDC Package 70515-115-06 Betapace Af

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:
70515-115-06
Package Description:
60 TABLET in 1 BOTTLE
Product Code:
70515-115
Proprietary Name:
Betapace Af
Usage Information:
This medication is used to treat a serious (possibly life-threatening) type of fast heartbeat called sustained ventricular tachycardia. It is also used to treat certain fast/irregular heartbeats (atrial fibrillation/flutter) in patients with severe symptoms such as weakness and shortness of breath. Sotalol helps to lessen these symptoms. It slows the heart rate and helps the heart to beat more normally and regularly. This medication is both a beta blocker and an anti-arrhythmic.
11-Digit NDC Billing Format:
70515011506
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:
Labeler Name:
Covis Pharma Us, Inc
Sample Package:
No
FDA Application Number:
NDA021151
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
09-01-2016
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.

Frequently Asked Questions

What is NDC 70515-115-06?

The NDC Packaged Code 70515-115-06 is assigned to a package of 60 tablet in 1 bottle of Betapace Af, labeled by Covis Pharma Us, Inc. The product's dosage form is and is administered via form.This product is billed for "EA" each discreet unit and contains an estimated amount of 60 billable units per package.

Is NDC 70515-115 included in the NDC Directory?

No, Betapace Af with product code 70515-115 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Covis Pharma Us, Inc on September 01, 2016 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 NDC billing unit for package 70515-115-06?

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 70515-115-06?

The 11-digit format is 70515011506. 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
5-3-270515-115-065-4-270515-0115-06