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  5. NDC Package Code: 51326-166-01 Womens Minoxidil Hair Regrowth

NDC Package 51326-166-01 Womens Minoxidil Hair Regrowth

Minoxidil Kit - 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:
51326-166-01
Package Description:
1 KIT in 1 CARTON * 200 mL in 1 BOTTLE * 200 mL in 1 BOTTLE * 60 mL in 1 BOTTLE (51326-161-01)
Product Code:
51326-166
Proprietary Name:
Womens Minoxidil Hair Regrowth
Non-Proprietary 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:
51326016601
NDC to RxNorm Crosswalk:
  • RxCUI: 311723 - minoxidil 2 % Topical Solution
  • RxCUI: 311723 - minoxidil 20 MG/ML Topical Solution
  • RxCUI: 311723 - minoxidil 2 GM per 100 ML Topical Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Topiderm, Inc
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    ANDA078176
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    06-16-2023
    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 51326-166-01?

    The NDC Packaged Code 51326-166-01 is assigned to a package of 1 kit in 1 carton * 200 ml in 1 bottle * 200 ml in 1 bottle * 60 ml in 1 bottle (51326-161-01) of Womens Minoxidil Hair Regrowth, a human over the counter drug labeled by Topiderm, Inc. The product's dosage form is kit and is administered via form.

    Is NDC 51326-166 included in the NDC Directory?

    Yes, Womens Minoxidil Hair Regrowth with product code 51326-166 is active and included in the NDC Directory. The product was first marketed by Topiderm, Inc on June 16, 2023 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 51326-166-01?

    The 11-digit format is 51326016601. 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
    5-3-251326-166-015-4-251326-0166-01