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  5. NDC Package Code: 71589-013-11 Testosterone

NDC Package 71589-013-11 Testosterone

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:
71589-013-11
Package Description:
1 BOTTLE, WITH APPLICATOR in 1 CARTON / 110 mL in 1 BOTTLE, WITH APPLICATOR
Product Code:
71589-013
Proprietary Name:
Testosterone
Usage Information:
This medicated gel contains testosterone. It is used for hormone replacement in men who are not able to produce enough testosterone (for example, due to hypogonadism). This medication is absorbed through the skin, enters your bloodstream, and helps your body reach normal testosterone levels. Testosterone helps the body to develop and maintain the male sexual characteristics (masculinity), such as a deep voice and body hair. It also helps to maintain muscle and prevent bone loss, and is necessary for natural sexual ability/desire. This drug should not be used by women.
11-Digit NDC Billing Format:
71589001311
NDC to RxNorm Crosswalk:
  • RxCUI: 1599949 - testosterone 2 % (30 MG/ACTUAT) Topical Solution, 60 ACTUAT
  • RxCUI: 1599949 - 60 ACTUAT testosterone 30 MG/ACTUAT Topical Solution
  • RxCUI: 1599949 - 60 ACTUAT testosterone 30 MG/1.5 ML ACTUAT Topical Solution
  • RxCUI: 1599949 - testosterone (as testosterone propionate) 2 % Topical Solution
    • Labeler Name:
    Aleor Dermaceuticals Limited
    Sample Package:
    No
    Start Marketing Date:
    07-01-2021
    Listing Expiration Date:
    12-31-2022
    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 71589-013-11?

    The NDC Packaged Code 71589-013-11 is assigned to a package of 1 bottle, with applicator in 1 carton / 110 ml in 1 bottle, with applicator of Testosterone, labeled by Aleor Dermaceuticals Limited. The product's dosage form is and is administered via form.

    Is NDC 71589-013 included in the NDC Directory?

    No, Testosterone with product code 71589-013 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Aleor Dermaceuticals Limited on July 01, 2021 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 71589-013-11?

    The 11-digit format is 71589001311. 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
    5-3-271589-013-115-4-271589-0013-11