NDC Package 50222-505-50 Finacea

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

Package Information
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:

50222-505-50

Package Description:

1 TUBE in 1 CARTON / 50 g in 1 TUBE

Product Code:

50222-505

Proprietary Name:

Finacea

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:

50222050550

Billing Unit:

GM - Billing unit of "gram" is used when a product is measured by its weight.

NDC to RxNorm Crosswalk:

50 GM

NDC to RxNorm Crosswalk:

RxCUI: 1041518 - azelaic acid 15 % Topical Gel
RxCUI: 1041518 - azelaic acid 0.15 MG/MG Topical Gel
RxCUI: 1043748 - Finacea 15 % Topical Gel
RxCUI: 1043748 - azelaic acid 0.15 MG/MG Topical Gel [Finacea]
RxCUI: 1043748 - Finacea 0.15 MG/MG Topical Gel

Product Type:

Human Prescription Drug

Labeler Name:

Leo Pharma Inc.

Dosage Form:

Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

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:

FDA Application Number:

NDA021470

Marketing Category:

NDA - A product marketed under an approved New Drug Application.

Start Marketing Date:

12-24-2002

End Marketing Date:

01-31-2026

Exclude Flag:

Code Structure:

50222 - Leo Pharma Inc.
- 50222-505 - Finacea
  - 50222-505-50 - 1 TUBE in 1 CARTON / 50 g in 1 TUBE

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 50222-505-50?

The NDC Packaged Code 50222-505-50 is assigned to a package of 1 tube in 1 carton / 50 g in 1 tube of Finacea, a human prescription drug labeled by Leo Pharma Inc.. The product's dosage form is gel and is administered via topical form.

Is NDC 50222-505 included in the NDC Directory?

Yes, Finacea with product code 50222-505 is active and included in the NDC Directory. The product was first marketed by Leo Pharma Inc. on December 24, 2002.

What is the NDC billing unit for package 50222-505-50?

The contents of this package are billed per "gm or gram", products billed per gram are products measured by weight. The calculated billable units for this package is 50.

What is the 11-digit format for NDC 50222-505-50?

The 11-digit format is 50222050550. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	50222-505-50	5-4-2	50222-0505-50

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