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  5. NDC Package Code: 68151-2958-0 Midodrine Hydrochloride

NDC Package 68151-2958-0 Midodrine Hydrochloride

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:
68151-2958-0
Package Description:
1 TABLET in 1 PACKAGE
Product Code:
68151-2958
Proprietary Name:
Midodrine Hydrochloride
Usage Information:
Midodrine hydrochloride tablets are indicated for the treatment of symptomatic orthostatic hypotension (OH). Because midodrine HCl can cause marked elevation of supine blood pressure (BP >200 mmHg systolic), it should be used in patients whose lives are considerably impaired despite standard clinical care, including non-pharmacologic treatment (such as support stockings), fluid expansion, and lifestyle alterations. The indication is based on midodrine HCl's effect on increases in 1-minute standing systolic blood pressure, a surrogate marker considered likely to correspond to a clinical benefit. At present, however, clinical benefits of midodrine HCl, principally improved ability to perform life activities, have not been established. Further clinical trials are underway to verify and describe the clinical benefits of midodrine HCl.After initiation of treatment, midodrine HCl tablets should be continued only for patients who report significant symptomatic improvement.
11-Digit NDC Billing Format:
68151295800
NDC to RxNorm Crosswalk:
  • RxCUI: 993470 - midodrine HCl 5 MG Oral Tablet
  • RxCUI: 993470 - midodrine hydrochloride 5 MG Oral Tablet
    • Labeler Name:
    Carilion Materials Management
    Sample Package:
    No
    Start Marketing Date:
    05-27-2004
    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 68151-2958-0?

    The NDC Packaged Code 68151-2958-0 is assigned to a package of 1 tablet in 1 package of Midodrine Hydrochloride, labeled by Carilion Materials Management. The product's dosage form is and is administered via form.

    Is NDC 68151-2958 included in the NDC Directory?

    No, Midodrine Hydrochloride with product code 68151-2958 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 May 27, 2004 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 68151-2958-0?

    The 11-digit format is 68151295800. 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
    5-4-168151-2958-05-4-268151-2958-00