Trichophyton For Intradermal Skin Testing
NDC Package 49643-128-01

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 inactivated by the FDA.

Trichophyton For Intradermal Skin Testing is a . Marketed by Allermed Laboratories, Inc., this product is identified by NDC 49643-128 and is authorized under FDA application BLA102211.

Identification & Billing

NDC Package Code
49643-128-01
Package Description
1 mL in 1 VIAL, MULTI-DOSE
Product Code
49643-128
11-Digit Billing Format
49643012801

Clinical Specifications

Proprietary Name
Trichophyton For Intradermal Skin Testing
Dosage Form
-

Regulatory & Marketing

Labeler Name
Allermed Laboratories, Inc.
FDA Application #
BLA102211
Marketing Category
BLA - A product marketed under an approved Biologic License Application.
Start Marketing Date
08-15-2007
Listing Expiration
12-31-2017
Exclude Flag
I
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 49643-128-01 identifies a specific commercial package of 1 ml in 1 vial, multi-dose of Trichophyton For Intradermal Skin Testing, labeled by Allermed Laboratories, 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 Allermed Laboratories, Inc. on August 15, 2007. The current certification is valid through December 31, 2017.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49643012801. 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)
49643-128-01
11-Digit CMS (5-4-2)
49643-0128-01

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