1. Home
  2. Labeler Index
  3. Actavis Pharma, Inc.
  4. 62037-833
  5. NDC Package Code: 62037-833-01 Metoprolol Succinate

NDC Package 62037-833-01 Metoprolol Succinate

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 .

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:
62037-833-01
Package Description:
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Code:
62037-833
Proprietary Name:
Metoprolol Succinate
Usage Information:
This medication is a beta-blocker used to treat chest pain (angina), heart failure, and high blood pressure. Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. This drug works by blocking the action of certain natural chemicals in your body (such as epinephrine) that affect the heart and blood vessels. This lowers heart rate, blood pressure, and strain on the heart.
11-Digit NDC Billing Format:
62037083301
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
100 EA
Labeler Name:
Actavis Pharma, Inc.
Sample Package:
No
FDA Application Number:
ANDA077298
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
04-15-2010
End Marketing Date:
01-31-2021
Listing Expiration Date:
01-31-2021
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 62037-833-01?

The NDC Packaged Code 62037-833-01 is assigned to a package of 100 tablet, film coated, extended release in 1 bottle, plastic of Metoprolol Succinate, labeled by Actavis Pharma, Inc.. The product's dosage form is and is administered via form.

Is NDC 62037-833 included in the NDC Directory?

The product was first marketed by Actavis Pharma, Inc. on April 15, 2010 and its listing in the NDC Directory is set to expire on January 31, 2021 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 62037-833-01?

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 100.

What is the 11-digit format for NDC 62037-833-01?

The 11-digit format is 62037083301. 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
5-3-262037-833-015-4-262037-0833-01