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  5. NDC Package Code: 68151-2701-0 Quinidine Gluconate

NDC Package 68151-2701-0 Quinidine Gluconate

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 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:
68151-2701-0
Package Description:
1 TABLET, EXTENDED RELEASE in 1 PACKAGE
Product Code:
68151-2701
Proprietary Name:
Quinidine Gluconate
Usage Information:
This medication is used to treat or prevent many types of irregular heartbeats (heart arrhythmias such as atrial fibrillation). Quinidine can greatly improve your ability to perform normal activities by decreasing the number of irregular heartbeats you have. However, it may not stop all your irregular heartbeats completely. It works by blocking abnormal heartbeat signals. Before and while you are using quinidine, your doctor may prescribe other medications (e.g., "blood thinners"/anticoagulants such as warfarin, beta blockers such as metoprolol) to shrink any blood clots in the heart and to slow your pulse.
11-Digit NDC Billing Format:
68151270100
NDC to RxNorm Crosswalk:
  • RxCUI: 852920 - quiNIDine gluconate 324 MG Extended Release Oral Tablet
  • RxCUI: 852920 - quinidine gluconate 324 MG Extended Release Oral Tablet
    • Labeler Name:
    Carilion Materials Management
    Sample Package:
    No
    Start Marketing Date:
    02-10-1987
    Listing Expiration Date:
    12-31-2018
    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 68151-2701-0?

    The NDC Packaged Code 68151-2701-0 is assigned to a package of 1 tablet, extended release in 1 package of Quinidine Gluconate, labeled by Carilion Materials Management. The product's dosage form is and is administered via form.

    Is NDC 68151-2701 included in the NDC Directory?

    No, Quinidine Gluconate with product code 68151-2701 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Carilion Materials Management on February 10, 1987 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 68151-2701-0?

    The 11-digit format is 68151270100. 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
    5-4-168151-2701-05-4-268151-2701-00