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  5. NDC Package Code: 63304-156-10 Benazepril Hydrochloride And Hydrochlorothiazide

NDC Package 63304-156-10 Benazepril Hydrochloride And Hydrochlorothiazide

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:
63304-156-10
Package Description:
1000 TABLET, COATED in 1 BOTTLE
Product Code:
63304-156
Proprietary Name:
Benazepril Hydrochloride And Hydrochlorothiazide
Usage Information:
Benazepril hydrochloride and hydrochlorothiazide tablets are indicated for the treatment of hypertension. This fixed combination drug is not indicated for the initial therapy of hypertension (see DOSAGE AND ADMINISTRATION).
11-Digit NDC Billing Format:
63304015610
NDC to RxNorm Crosswalk:
  • RxCUI: 898362 - benazepril HCl 10 MG / hydroCHLOROthiazide 12.5 MG Oral Tablet
  • RxCUI: 898362 - benazepril hydrochloride 10 MG / hydrochlorothiazide 12.5 MG Oral Tablet
  • RxCUI: 898362 - benazepril hydrochloride 10 MG / HCTZ 12.5 MG Oral Tablet
  • RxCUI: 898362 - BZP hydrochloride 10 MG / HCTZ 12.5 MG Oral Tablet
  • RxCUI: 898367 - benazepril HCl 20 MG / hydroCHLOROthiazide 12.5 MG Oral Tablet
    • Labeler Name:
    Ranbaxy Pharmaceuticals Inc.
    Sample Package:
    No
    Start Marketing Date:
    04-10-2006
    Listing Expiration Date:
    12-31-2019
    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
    63304-156-01100 TABLET, COATED in 1 BOTTLE
    63304-156-3030 TABLET, COATED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 63304-156-10?

    The NDC Packaged Code 63304-156-10 is assigned to a package of 1000 tablet, coated in 1 bottle of Benazepril Hydrochloride And Hydrochlorothiazide, labeled by Ranbaxy Pharmaceuticals Inc.. The product's dosage form is and is administered via form.

    Is NDC 63304-156 included in the NDC Directory?

    No, Benazepril Hydrochloride And Hydrochlorothiazide with product code 63304-156 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Ranbaxy Pharmaceuticals Inc. on April 10, 2006 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 63304-156-10?

    The 11-digit format is 63304015610. 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
    5-3-263304-156-105-4-263304-0156-10