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  5. NDC Package Code: 61200-037-02 Ingenol Mebutate

NDC Package 61200-037-02 Ingenol Mebutate

Powder, For Suspension - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

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:
61200-037-02
Package Description:
.006 kg in 1 DRUM
Product Code:
61200-037
Non-Proprietary Name:
Ingenol Mebutate
Substance Name:
Ingenol Mebutate
Usage Information:
This medication is used on the skin to treat pre-cancerous and cancerous skin growths. Talk to your doctor about the risks and benefits of ingenol, as well as alternative treatments for your condition. It is not known exactly how ingenol works, but it can kill abnormal cells that cause skin cancer.
11-Digit NDC Billing Format:
61200003702
Product Type:
Bulk Ingredient
Labeler Name:
Sichuan Xieli Pharmaceutical Co., Ltd.
Dosage Form:
Powder, For Suspension - An intimate mixture of dry, finely divided drugs and/or chemicals, which, upon the addition of suitable vehicles, yields a suspension (a liquid preparation containing the solid particles dispersed in the liquid vehicle).
Active Ingredient(s):
  • INGENOL MEBUTATE 1 kg/kg
    • Sample Package:
    N/A
    Marketing Category:
    BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING - A category specifying that a bulk product is intended for use on humans and requires a prescription.
    Start Marketing Date:
    10-25-2019
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Unfinished Product:
    Yes
    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 61200-037-02?

    The NDC Packaged Code 61200-037-02 is assigned to an UNFINISHED drug package of .006 kg in 1 drum of Ingenol Mebutate, a bulk ingredient labeled by Sichuan Xieli Pharmaceutical Co., Ltd.. The product's dosage form is powder, for suspension and is administered via form.

    Is NDC 61200-037 included in the NDC Directory?

    Yes, Ingenol Mebutate is an UNFINISHED PRODUCT with code 61200-037 that is active and included in the NDC Directory. The product was first marketed by Sichuan Xieli Pharmaceutical Co., Ltd. on October 25, 2019 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 11-digit format for NDC 61200-037-02?

    The 11-digit format is 61200003702. 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
    5-3-261200-037-025-4-261200-0037-02