NDC Package 70934-113-30 Metoprolol Succinate

View Billable Units, 11-Digit Format, RxNorm

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:
70934-113-30
Package Description:
30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Code:
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:
70934011330
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
30 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 866427 - metoprolol succinate 25 MG 24HR Extended Release Oral Tablet
  • RxCUI: 866427 - 24 HR metoprolol succinate 25 MG Extended Release Oral Tablet
  • RxCUI: 866427 - 24 HR metoprolol succinate 25 MG (as metoprolol succinate 23.75 MG equivalent to 25 MG metoprolol tartrate) Extended Release Oral Tablet
  • RxCUI: 866427 - metoprolol succinate 25 MG 24 HR Extended Release Oral Tablet
  • Labeler Name:
    Denton Pharma, Inc. Dba Northwind Pharmaceuticals
    Sample Package:
    No
    Start Marketing Date:
    05-09-2018
    Listing Expiration Date:
    12-31-2019
    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 70934-113-30?

    The NDC Packaged Code 70934-113-30 is assigned to a package of 30 tablet, extended release in 1 bottle, plastic of Metoprolol Succinate, labeled by Denton Pharma, Inc. Dba Northwind Pharmaceuticals. 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 30 billable units per package.

    Is NDC 70934-113 included in the NDC Directory?

    No, Metoprolol Succinate with product code 70934-113 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Denton Pharma, Inc. Dba Northwind Pharmaceuticals on May 09, 2018 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 70934-113-30?

    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 30.

    What is the 11-digit format for NDC 70934-113-30?

    The 11-digit format is 70934011330. 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
    5-3-270934-113-305-4-270934-0113-30