NDC Package 68071-4144-6 Enalapril Maleate And Hydrochlorothiazide

View Billable Units, 11-Digit Format, RxNorm

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:
68071-4144-6
Package Description:
60 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Enalapril Maleate And Hydrochlorothiazide
Usage Information:
Enalapril maleate and hydrochlorothiazide is indicated for the treatment of hypertension.This fixed dose combination is not indicated for initial treatment (see DOSAGE AND ADMINISTRATION). In using enalapril maleate and hydrochlorothiazide, consideration should be given to the fact that another angiotensin converting enzyme inhibitor, captopril, has caused agranulocytosis, particularly in patients with renal impairment or collagen vascular disease, and that available data are insufficient to show that enalapril does not have a similar risk (see WARNINGS). In considering use of enalapril maleate and hydrochlorothiazide, it should be noted that black patients receiving ACE inhibitors have been reported to have a higher incidence of angioedema compared to non-blacks (see WARNINGS, Head and Neck Angioedema).
11-Digit NDC Billing Format:
68071414406
NDC to RxNorm Crosswalk:
  • RxCUI: 858828 - enalapril maleate 10 MG / hydroCHLOROthiazide 25 MG Oral Tablet
  • RxCUI: 858828 - enalapril maleate 10 MG / hydrochlorothiazide 25 MG Oral Tablet
  • RxCUI: 858828 - enalapril maleate 10 MG / HCTZ 25 MG Oral Tablet
  • Labeler Name:
    Nucare Pharmaceuticals,inc.
    Sample Package:
    No
    Start Marketing Date:
    09-18-2001
    Listing Expiration Date:
    12-31-2022
    Exclude Flag:
    I

    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
    68071-4144-330 TABLET in 1 BOTTLE
    68071-4144-990 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 68071-4144-6?

    The NDC Packaged Code 68071-4144-6 is assigned to a package of 60 tablet in 1 bottle of Enalapril Maleate And Hydrochlorothiazide, labeled by Nucare Pharmaceuticals,inc.. The product's dosage form is and is administered via form.

    Is NDC 68071-4144 included in the NDC Directory?

    No, Enalapril Maleate And Hydrochlorothiazide with product code 68071-4144 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Nucare Pharmaceuticals,inc. on September 18, 2001 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 68071-4144-6?

    The 11-digit format is 68071414406. 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
    5-4-168071-4144-65-4-268071-4144-06