Dermataf Antifungal Treatment
NDC Package 50080-002-15

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Dermataf Antifungal Treatment is a . Marketed by Dermataf, Inc., this product is identified by NDC 50080-002 and is authorized under FDA application part333C.

Identification & Billing

NDC Package Code
50080-002-15
Package Description
1 BOTTLE in 1 BOX / 15 mL in 1 BOTTLE
Product Code
50080-002
11-Digit Billing Format
50080000215

Clinical Specifications

Proprietary Name
Dermataf Antifungal Treatment
Dosage Form
-

Regulatory & Marketing

Labeler Name
Dermataf, Inc.
FDA Application #
part333C
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
01-15-2013
End Marketing Date
03-04-2015
Listing Expiration
03-04-2015
Exclude Flag
D
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 50080-002-15 identifies a specific commercial package of 1 bottle in 1 box / 15 ml in 1 bottle of Dermataf Antifungal Treatment, labeled by Dermataf, Inc.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Dermataf, Inc. on January 15, 2013. The current certification is valid through March 04, 2015.

How is this Dermataf, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50080000215. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
50080-002-15
11-Digit CMS (5-4-2)
50080-0002-15

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.