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  5. NDC Package Code: 70518-2139-0 Nadolol

NDC Package 70518-2139-0 Nadolol

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:
70518-2139-0
Package Description:
90 TABLET in 1 BOTTLE, PLASTIC
Product Code:
70518-2139
Proprietary Name:
Nadolol
Usage Information:
Nadolol is used alone or with other medications to treat high blood pressure (hypertension) and to prevent chest pain (angina). Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. In the management of chest pain, nadolol may also help to reduce the frequency of chest pain episodes and improve your ability to exercise. Nadolol belongs to a class of medications called beta blockers. It works by blocking the action of certain natural substances such as adrenaline (epinephrine) on the heart and blood vessels. This results in a lowering of heart rate, blood pressure, and strain on the heart.
11-Digit NDC Billing Format:
70518213900
Labeler Name:
Remedyrepack Inc.
Sample Package:
No
FDA Application Number:
ANDA207761
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
06-10-2019
End Marketing Date:
04-11-2024
Listing Expiration Date:
04-11-2024
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 70518-2139-0?

The NDC Packaged Code 70518-2139-0 is assigned to a package of 90 tablet in 1 bottle, plastic of Nadolol, labeled by Remedyrepack Inc.. The product's dosage form is and is administered via form.

Is NDC 70518-2139 included in the NDC Directory?

No, Nadolol with product code 70518-2139 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Remedyrepack Inc. on June 10, 2019 and its listing in the NDC Directory is set to expire on April 11, 2024 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 70518-2139-0?

The 11-digit format is 70518213900. 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
5-4-170518-2139-05-4-270518-2139-00