NDC Package 83767-002-01 5% Minoxidil Foam

Minoxidil Aerosol, Foam Topical - View Billable Units, 11-Digit Format, RxNorm

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:
83767-002-01
Package Description:
2 BOTTLE in 1 PACKAGE / 60 g in 1 BOTTLE
Product Code:
Proprietary Name:
5% Minoxidil Foam
Non-Proprietary Name:
Minoxidil
Substance Name:
Biotin; 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:
83767000201
Product Type:
Human Otc Drug
Labeler Name:
Guangzhou Ruijiu Electronic Technology Co., Ltd.
Dosage Form:
Aerosol, Foam - A dosage form containing one or more active ingredients, surfactants, aqueous or nonaqueous liquids, and the propellants; if the propellant is in the internal (discontinuous) phase (i.e., of the oil-in-water type), a stable foam is discharged, and if the propellant is in the external (continuous) phase (i.e., of the water-in-oil type), a spray or a quick-breaking foam is discharged.
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):
Sample Package:
No
FDA Application Number:
505G(a)(3)
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
09-12-2024
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.

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Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
83767-002-023 BOTTLE in 1 PACKAGE / 60 g in 1 BOTTLE

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Frequently Asked Questions

What is NDC 83767-002-01?

The NDC Packaged Code 83767-002-01 is assigned to a package of 2 bottle in 1 package / 60 g in 1 bottle of 5% Minoxidil Foam, a human over the counter drug labeled by Guangzhou Ruijiu Electronic Technology Co., Ltd.. The product's dosage form is aerosol, foam and is administered via topical form.

Is NDC 83767-002 included in the NDC Directory?

Yes, 5% Minoxidil Foam with product code 83767-002 is active and included in the NDC Directory. The product was first marketed by Guangzhou Ruijiu Electronic Technology Co., Ltd. on September 12, 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 83767-002-01?

The 11-digit format is 83767000201. 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
5-3-283767-002-015-4-283767-0002-01