NDC Package 70518-2052-0 Tamsulosin Hydrochloride

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

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:
70518-2052-0
Package Description:
90 CAPSULE in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Tamsulosin Hydrochloride
Non-Proprietary Name:
Tamsulosin Hydrochloride
Substance Name:
Tamsulosin Hydrochloride
Usage Information:
Tamsulosin hydrochloride capsules are indicated for the treatment of the signs and symptoms of benign prostatic hyperplasia (BPH) [see Clinical Studies (14)] . Tamsulosin hydrochloride capsules are not indicated for the treatment of hypertension.
11-Digit NDC Billing Format:
70518205200
NDC to RxNorm Crosswalk:
  • RxCUI: 863669 - tamsulosin HCl 0.4 MG Oral Capsule
  • RxCUI: 863669 - tamsulosin hydrochloride 0.4 MG Oral Capsule
  • RxCUI: 863669 - tamsulosin HCl 0.4 MG Modified Release Oral Capsule
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Remedyrepack Inc.
    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):
    Sample Package:
    No
    FDA Application Number:
    ANDA202433
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    04-30-2019
    Listing Expiration Date:
    12-31-2025
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    70518-2052-130 CAPSULE in 1 BLISTER PACK

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70518-2052-0?

    The NDC Packaged Code 70518-2052-0 is assigned to a package of 90 capsule in 1 bottle, plastic of Tamsulosin Hydrochloride, a human prescription drug labeled by Remedyrepack Inc.. The product's dosage form is capsule and is administered via oral form.

    Is NDC 70518-2052 included in the NDC Directory?

    Yes, Tamsulosin Hydrochloride with product code 70518-2052 is active and included in the NDC Directory. The product was first marketed by Remedyrepack Inc. on April 30, 2019 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 70518-2052-0?

    The 11-digit format is 70518205200. 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
    5-4-170518-2052-05-4-270518-2052-00