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  5. NDC Package Code: 0024-5837-01 Flomax

NDC Package 0024-5837-01 Flomax

Tamsulosin Hydrochloride Capsule Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

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:
0024-5837-01
Package Description:
100 CAPSULE in 1 BOTTLE
Product Code:
0024-5837
Proprietary Name:
Flomax
Non-Proprietary Name:
Tamsulosin Hydrochloride
Substance Name:
Tamsulosin Hydrochloride
Usage Information:
Tamsulosin is used by men to treat the symptoms of an enlarged prostate (benign prostatic hyperplasia-BPH). It does not shrink the prostate, but it works by relaxing the muscles in the prostate and the bladder. This helps to relieve symptoms of BPH such as difficulty in beginning the flow of urine, weak stream, and the need to urinate often or urgently (including during the middle of the night). Tamsulosin belongs to a class of drugs known as alpha blockers. Do not use this medication to treat high blood pressure.
11-Digit NDC Billing Format:
00024583701
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
100 EA
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Sanofi-aventis U.s. Llc
Dosage Form:
Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
TAMSULOSIN HYDROCHLORIDE .4 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
NDA020579
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
09-12-1997
End Marketing Date:
10-31-2025
Exclude Flag:
N
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 0024-5837-01?

The NDC Packaged Code 0024-5837-01 is assigned to a package of 100 capsule in 1 bottle of Flomax, a human prescription drug labeled by Sanofi-aventis U.s. Llc. The product's dosage form is capsule and is administered via oral form.

Is NDC 0024-5837 included in the NDC Directory?

Yes, Flomax with product code 0024-5837 is active and included in the NDC Directory. The product was first marketed by Sanofi-aventis U.s. Llc on September 12, 1997.

What is the NDC billing unit for package 0024-5837-01?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 100.

What is the 11-digit format for NDC 0024-5837-01?

The 11-digit format is 00024583701. 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 4-4-2 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
4-4-20024-5837-015-4-200024-5837-01