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  5. NDC Package Code: 82372-009-01 5% Minoxidil Hair Regrowth Kit

NDC Package 82372-009-01 5% Minoxidil Hair Regrowth Kit

Hair Loss Product Liquid Topical - 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:
82372-009-01
Package Description:
60 mL in 1 BOTTLE
Product Code:
82372-009
Proprietary Name:
5% Minoxidil Hair Regrowth Kit
Non-Proprietary Name:
Hair Loss Product
Substance Name:
Minoxidil
Usage Information:
Minoxidil is used with other medications to treat high blood pressure (hypertension). Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. Minoxidil works by relaxing blood vessels so blood can flow more easily.
11-Digit NDC Billing Format:
82372000901
Product Type:
Human Otc Drug
Labeler Name:
Good Manager Holdings Inc
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Active Ingredient(s):
  • MINOXIDIL 5 mg/100mL
    • Pharmacologic Class(es):
  • Arteriolar Vasodilation - [PE] (Physiologic Effect)
  • Arteriolar Vasodilator - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA075357
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    02-23-2024
    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.

    Frequently Asked Questions

    What is NDC 82372-009-01?

    The NDC Packaged Code 82372-009-01 is assigned to a package of 60 ml in 1 bottle of 5% Minoxidil Hair Regrowth Kit, a human over the counter drug labeled by Good Manager Holdings Inc. The product's dosage form is liquid and is administered via topical form.

    Is NDC 82372-009 included in the NDC Directory?

    Yes, 5% Minoxidil Hair Regrowth Kit with product code 82372-009 is active and included in the NDC Directory. The product was first marketed by Good Manager Holdings Inc on February 23, 2024 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 82372-009-01?

    The 11-digit format is 82372000901. 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
    5-3-282372-009-015-4-282372-0009-01