NDC Package 49643-128-01 Trichophyton For Intradermal Skin Testing

View Billable Units, 11-Digit Format, RxNorm

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:
49643-128-01
Package Description:
1 mL in 1 VIAL, MULTI-DOSE
Product Code:
Proprietary Name:
Trichophyton For Intradermal Skin Testing
Usage Information:
Intradermal skin tests with Trichophyton extract are indicated for use in persons who are suspected of having Type I hypersensitivity (i.e. allergy) to the fungus.
11-Digit NDC Billing Format:
49643012801
NDC to RxNorm Crosswalk:
  • RxCUI: 485356 - Trichophyton antigen 2 MG/mL Injectable Solution
  • RxCUI: 485356 - Trichophyton antigen 2 MG/ML Injectable Solution
  • Labeler Name:
    Allermed Laboratories, Inc.
    Sample Package:
    No
    Start Marketing Date:
    08-15-2007
    Listing Expiration Date:
    12-31-2017
    Exclude Flag:
    I

    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 49643-128-01?

    The NDC Packaged Code 49643-128-01 is assigned to a package of 1 ml in 1 vial, multi-dose of Trichophyton For Intradermal Skin Testing, labeled by Allermed Laboratories, Inc.. The product's dosage form is and is administered via form.

    Is NDC 49643-128 included in the NDC Directory?

    No, Trichophyton For Intradermal Skin Testing with product code 49643-128 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Allermed Laboratories, Inc. on August 15, 2007 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 49643-128-01?

    The 11-digit format is 49643012801. 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
    5-3-249643-128-015-4-249643-0128-01