Alfuzosin Hydrochloride Tablet, Extended Release
NDC Package 63629-9155-2

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Alfuzosin Hydrochloride tablets is alfuzosin hydrochloride extended-release tablets, USP are not indicated for the treatment of hypertension. This formulation utilizes a tablet, extended release delivery system. Marketed by Bryant Ranch Prepack, this product is identified by NDC 63629-9155 and is authorized under FDA application ANDA203192.

Identification & Billing

NDC Package Code
63629-9155-2
Package Description
60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Code
63629-9155
11-Digit Billing Format
63629915502
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

Clinical Specifications

Proprietary Name
Alfuzosin Hydrochloride
Non-Proprietary Name
Alfuzosin Hydrochloride
Substance Name
Alfuzosin Hydrochloride
Dosage Form
Tablet, Extended Release - A solid dosage form containing a drug which allows at least a reduction in dosing frequency as compared to that drug presented in conventional dosage form.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
ALFUZOSIN HYDROCHLORIDE 10 mg/1
Pharmacologic Class
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.

Regulatory & Marketing

Labeler Name
Bryant Ranch Prepack
Product Type
Human Prescription Drug
FDA Application #
ANDA203192
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
03-15-2016
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (63629-9155). Click a package code to view its specific billing and regulatory data.

63629-9155-1
30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
63629-9155-3
90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
63629-9155-4
120 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 63629-9155-2 identifies a specific commercial package of 60 tablet, extended release in 1 bottle, plastic of Alfuzosin Hydrochloride, a human prescription drug labeled by Bryant Ranch Prepack. This tablet, extended release is formulated for oral use and contains alfuzosin hydrochloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Bryant Ranch Prepack on March 15, 2016. The current certification is valid through December 31, 2026.

How is this Bryant Ranch Prepack product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 63629915502. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
63629-9155-2
11-Digit CMS (5-4-2)
63629-9155-02

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.