Pediaderm Ta
NDC Package 24338-430-01

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.

Pediaderm Ta is triamcinolone acetonide cream is indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses. Marketed by Arbor Pharmaceuticals, Inc., this product is identified by NDC 24338-430 and is authorized under FDA application ANDA040039.

Identification & Billing

NDC Package Code
24338-430-01
Package Description
1 TUBE in 1 KIT / 30 g in 1 TUBE
Product Code
24338-430
11-Digit Billing Format
24338043001
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Pediaderm Ta
Dosage Form
-
Usage Information
Triamcinolone acetonide cream is indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

Regulatory & Marketing

Labeler Name
Arbor Pharmaceuticals, Inc.
FDA Application #
ANDA040039
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
09-01-2010
Listing Expiration
12-31-2018
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 24338-430-01 identifies a specific commercial package of 1 tube in 1 kit / 30 g in 1 tube of Pediaderm Ta, labeled by Arbor Pharmaceuticals, 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 Arbor Pharmaceuticals, Inc. on September 01, 2010. The current certification is valid through December 31, 2018.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 24338043001. 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)
24338-430-01
11-Digit CMS (5-4-2)
24338-0430-01

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