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  5. NDC Package Code: 49539-001-01 5% Minoxidil Topical Solution

NDC Package 49539-001-01 5% Minoxidil Topical Solution

Minoxidil Solution 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:
49539-001-01
Package Description:
3 BOTTLE in 1 CARTON / 60 mL in 1 BOTTLE
Product Code:
49539-001
Proprietary Name:
5% Minoxidil Topical Solution
Non-Proprietary Name:
Minoxidil
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:
49539000101
NDC to RxNorm Crosswalk:
  • RxCUI: 311724 - minoxidil 5 % Topical Solution
  • RxCUI: 311724 - minoxidil 50 MG/ML Topical Solution
  • RxCUI: 311724 - minoxidil 3 GM per 60 ML Topical Solution
  • RxCUI: 311724 - minoxidil 5 GM per 100 ML Topical Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Avacor Products, Llc
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    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 g/100mL
    • Pharmacologic Class(es):
  • Arteriolar Vasodilation - [PE] (Physiologic Effect)
  • Arteriolar Vasodilator - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA076239
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    04-01-2019
    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 49539-001-01?

    The NDC Packaged Code 49539-001-01 is assigned to a package of 3 bottle in 1 carton / 60 ml in 1 bottle of 5% Minoxidil Topical Solution, a human over the counter drug labeled by Avacor Products, Llc. The product's dosage form is solution and is administered via topical form.

    Is NDC 49539-001 included in the NDC Directory?

    Yes, 5% Minoxidil Topical Solution with product code 49539-001 is active and included in the NDC Directory. The product was first marketed by Avacor Products, Llc on April 01, 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 49539-001-01?

    The 11-digit format is 49539000101. 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
    5-3-249539-001-015-4-249539-0001-01