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  5. NDC Package Code: 51655-535-52 Metoprolol Tartate

NDC Package 51655-535-52 Metoprolol Tartate

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
51655-535-52
Package Description:
30 TABLET in 1 BOTTLE, DISPENSING
Product Code:
51655-535
Proprietary Name:
Metoprolol Tartate
Usage Information:
Hypertension and AnginaMetoprolol tartrate is contraindicated in sinus bradycardia, heart block greater than first degree, cardiogenic shock, and overt cardiac failure (see WARNINGS).Hypersensitivity to metoprolol and related derivatives, or to any of the excipients; hypersensitivity to other beta-blockers (cross sensitivity between beta-blockers can occur).Sick-sinus syndrome.Severe peripheral arterial circulatory disorders.Myocardial InfarctionMetoprolol is contraindicated in patients with a heart rate < 45 beats/min; second- and third-degree heart block; significant first-degree heart block (P-R interval ≥ 0.24 sec); systolic blood pressure < 100 mmHg; or moderate-to-severe cardiac failure (see WARNINGS).
11-Digit NDC Billing Format:
51655053552
NDC to RxNorm Crosswalk:
  • RxCUI: 866514 - metoprolol tartrate 50 MG Oral Tablet
    • Labeler Name:
    Northwind Pharmaceuticals
    Sample Package:
    No
    Start Marketing Date:
    06-02-2014
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    51655-535-2560 TABLET in 1 BOTTLE, DISPENSING
    51655-535-2690 TABLET in 1 BOTTLE, DISPENSING

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 51655-535-52?

    The NDC Packaged Code 51655-535-52 is assigned to a package of 30 tablet in 1 bottle, dispensing of Metoprolol Tartate, labeled by Northwind Pharmaceuticals. The product's dosage form is and is administered via form.

    Is NDC 51655-535 included in the NDC Directory?

    No, Metoprolol Tartate with product code 51655-535 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Northwind Pharmaceuticals on June 02, 2014 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 11-digit format for NDC 51655-535-52?

    The 11-digit format is 51655053552. 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
    5-3-251655-535-525-4-251655-0535-52