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  5. NDC Package Code: 50090-1336-0 Aplisol

NDC Package 50090-1336-0 Aplisol

Tuberculin Purified Protein Derivative Injection Intradermal - 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:
50090-1336-0
Package Description:
1 VIAL in 1 CARTON / 1 mL in 1 VIAL
Product Code:
50090-1336
Proprietary Name:
Aplisol
Non-Proprietary Name:
Tuberculin Purified Protein Derivative
Substance Name:
Tuberculin Purified Protein Derivative
Usage Information:
Tuberculin PPD is indicated as an aid in the detection of infection with Mycobacterium tuberculosis. The standard tuberculin test employs the intradermal (Mantoux) test using a 5 TU dose of tuberculin PPD.7 The 0.1 mL test dose of Aplisol (tuberculin PPD, diluted) is equivalent to the 5 TU dose which has been clinically utilized and standardized with PPD-S. Tuberculin skin testing is not contraindicated for persons who have been vaccinated with BCG and the skin-test results of such persons are used to support or exclude the diagnosis of M. tuberculosis infections.4 HIV infection is a strong risk factor for the development of TB disease in persons having TB infection. All HIV-infected persons should receive a PPD-tuberculin skin test.3
11-Digit NDC Billing Format:
50090133600
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 313532 - purified protein derivative of tuberculin 5 UNT in 0.1 ML Injectable Solution
  • RxCUI: 313532 - purified protein derivative of tuberculin 50 UNT/ML Injectable Solution
  • RxCUI: 313532 - purified protein derivative of tuberculin 5 UNT per 0.1 ML Injectable Solution
  • RxCUI: 798408 - Aplisol 5 UNT in 0.1 ML Injectable Solution
  • RxCUI: 798408 - purified protein derivative of tuberculin 50 UNT/ML Injectable Solution [Aplisol]
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    A-s Medication Solutions
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Intradermal - Administration within the dermis.
    • Active Ingredient(s):
  • TUBERCULIN PURIFIED PROTEIN DERIVATIVE 5 [iU]/.1mL
    • Pharmacologic Class(es):
  • Antigens, Bacterial - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Skin Test Antigen - [EPC] (Established Pharmacologic Class)
  • Tuberculosis Skin Test - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    BLA103782
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    04-25-2008
    Listing Expiration Date:
    12-31-2024
    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 50090-1336-0?

    The NDC Packaged Code 50090-1336-0 is assigned to a package of 1 vial in 1 carton / 1 ml in 1 vial of Aplisol, a human prescription drug labeled by A-s Medication Solutions. The product's dosage form is injection and is administered via intradermal form.

    Is NDC 50090-1336 included in the NDC Directory?

    Yes, Aplisol with product code 50090-1336 is active and included in the NDC Directory. The product was first marketed by A-s Medication Solutions on April 25, 2008 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 50090-1336-0?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 50090-1336-0?

    The 11-digit format is 50090133600. 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
    5-4-150090-1336-05-4-250090-1336-00