1. Home
  2. Labeler Index
  3. Bryant Ranch Prepack
  4. 63629-7907
  5. NDC Package Code: 63629-7907-1 Alfuzosin Hydrochloride

NDC Package 63629-7907-1 Alfuzosin 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:
63629-7907-1
Package Description:
90 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Code:
63629-7907
Proprietary Name:
Alfuzosin Hydrochloride
Usage Information:
Alfuzosin hydrochloride extended-release tablets, USP are not indicated for the treatment of hypertension. Alfuzosin hydrochloride extended-release tablets, USP are not indicated for use in pediatric population.
11-Digit NDC Billing Format:
63629790701
NDC to RxNorm Crosswalk:
  • RxCUI: 861132 - alfuzosin HCl 10 MG 24HR Extended Release Oral Tablet
  • RxCUI: 861132 - 24 HR alfuzosin hydrochloride 10 MG Extended Release Oral Tablet
  • RxCUI: 861132 - alfuzosin hydrochloride 10 MG 24 HR Extended Release Oral Tablet
    • Labeler Name:
    Bryant Ranch Prepack
    Sample Package:
    No
    FDA Application Number:
    ANDA203192
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    03-15-2016
    Listing Expiration Date:
    12-31-2023
    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 63629-7907-1?

    The NDC Packaged Code 63629-7907-1 is assigned to a package of 90 tablet, extended release in 1 bottle of Alfuzosin Hydrochloride, labeled by Bryant Ranch Prepack. The product's dosage form is and is administered via form.

    Is NDC 63629-7907 included in the NDC Directory?

    No, Alfuzosin Hydrochloride with product code 63629-7907 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Bryant Ranch Prepack on March 15, 2016 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 63629-7907-1?

    The 11-digit format is 63629790701. 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
    5-4-163629-7907-15-4-263629-7907-01