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  5. NDC Package Code: 50222-303-91 Finacea Foam

NDC Package 50222-303-91 Finacea Foam

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

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
50222-303-91
Package Description:
1 CAN in 1 CARTON / 15 g in 1 CAN
Product Code:
50222-303
Proprietary Name:
Finacea Foam
Non-Proprietary Name:
Azelaic Acid
Substance Name:
Azelaic Acid
Usage Information:
This medication is used to treat a certain skin condition called rosacea. It helps to reduce the number of inflamed skin lesions.
11-Digit NDC Billing Format:
50222030391
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Leo Pharma Inc.
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):
AZELAIC ACID .15 g/g
Pharmacologic Class(es):
Sample Package:
Yes
FDA Application Number:
NDA207071
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
10-01-2018
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
50222-303-501 CAN in 1 CARTON / 50 g in 1 CAN

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 50222-303-91?

The NDC Packaged Code 50222-303-91 is assigned to a package of 1 can in 1 carton / 15 g in 1 can of Finacea Foam, a human prescription drug labeled by Leo Pharma Inc.. The product's dosage form is aerosol, foam and is administered via topical form.

Is NDC 50222-303 included in the NDC Directory?

Yes, Finacea Foam with product code 50222-303 is active and included in the NDC Directory. The product was first marketed by Leo Pharma Inc. on October 01, 2018 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 50222-303-91?

The 11-digit format is 50222030391. 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
5-3-250222-303-915-4-250222-0303-91