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  5. NDC Package Code: 70934-797-30 Clopidogrel Bisulfate

NDC Package 70934-797-30 Clopidogrel Bisulfate

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:
70934-797-30
Package Description:
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Code:
70934-797
Proprietary Name:
Clopidogrel Bisulfate
Usage Information:
• Clopidogrel is indicated to reduce the rate of myocardial infarction (MI) and stroke in patients with non–ST-segment elevation ACS (unstable angina [UA]/ non–ST -elevation myocardial infarction [NSTEMI]), including patients who are to be managed medically and those who are to be managed with coronary revascularization. Clopidogrel should be administered in conjunction with aspirin. • Clopidogrel is indicated to reduce the rate of myocardial infarction and stroke in patients with acute ST-elevation myocardial infarction (STEMI) who are to be managed medically. Clopidogrel should be administered in conjunction with aspirin.
11-Digit NDC Billing Format:
70934079730
NDC to RxNorm Crosswalk:
  • RxCUI: 309362 - clopidogrel 75 MG Oral Tablet
  • RxCUI: 309362 - clopidogrel 75 MG (as clopidogrel bisulfate 97.875 MG) Oral Tablet
    • Labeler Name:
    Denton Pharma, Inc. Dba Northwind Pharmaceuticals
    Sample Package:
    No
    Start Marketing Date:
    11-09-2020
    Listing Expiration Date:
    12-31-2022
    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
    70934-797-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70934-797-30?

    The NDC Packaged Code 70934-797-30 is assigned to a package of 30 tablet, film coated in 1 bottle, plastic of Clopidogrel Bisulfate, labeled by Denton Pharma, Inc. Dba Northwind Pharmaceuticals. The product's dosage form is and is administered via form.

    Is NDC 70934-797 included in the NDC Directory?

    No, Clopidogrel Bisulfate with product code 70934-797 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 November 09, 2020 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 70934-797-30?

    The 11-digit format is 70934079730. 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
    5-3-270934-797-305-4-270934-0797-30