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  5. NDC Package Code: 68151-1472-0 Moexipril Hydrochloride

NDC Package 68151-1472-0 Moexipril 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:
68151-1472-0
Package Description:
1 TABLET, FILM COATED in 1 PACKAGE
Product Code:
68151-1472
Proprietary Name:
Moexipril Hydrochloride
Usage Information:
Moexipril hydrochloride tablets USP are indicated for treatment of patients with hypertension. It may be used alone or in combination with thiazide diuretics.In using moexipril hydrochloride tablets USP, consideration should be given to the fact that another ACE inhibitor, captopril, has caused agranulocytosis, particularly in patients with renal impairment or collagen-vascular disease. Available data are insufficient to show that moexipril hydrochloride tablets USP do not have a similar risk (see WARNINGS).In considering use of moexipril hydrochloride tablets USP, it should be noted that in controlled trials ACE inhibitors have an effect on blood pressure that is less in black patients than in non-blacks. In addition, ACE inhibitors (for which adequate data are available) cause a higher rate of angioedema in black than in non-black patients (see WARNINGS,Angioedema).
11-Digit NDC Billing Format:
68151147200
NDC to RxNorm Crosswalk:
  • RxCUI: 1299896 - moexipril HCl 15 MG Oral Tablet
  • RxCUI: 1299896 - moexipril hydrochloride 15 MG Oral Tablet
  • RxCUI: 1299897 - moexipril HCl 7.5 MG Oral Tablet
  • RxCUI: 1299897 - moexipril hydrochloride 7.5 MG Oral Tablet
    • Labeler Name:
    Carilion Materials Management
    Sample Package:
    No
    Start Marketing Date:
    05-08-2003
    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 68151-1472-0?

    The NDC Packaged Code 68151-1472-0 is assigned to a package of 1 tablet, film coated in 1 package of Moexipril Hydrochloride, labeled by Carilion Materials Management. The product's dosage form is and is administered via form.

    Is NDC 68151-1472 included in the NDC Directory?

    No, Moexipril Hydrochloride with product code 68151-1472 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 08, 2003 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 68151-1472-0?

    The 11-digit format is 68151147200. 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
    5-4-168151-1472-05-4-268151-1472-00