Otis Clapp Ultraprin
NDC Package 47682-080-13

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

Package Information

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

Otis Clapp Ultraprin is a . Marketed by Unifirst First Aid Corporation, this product is identified by NDC 47682-080 and is authorized under FDA application ANDA071333.

Identification & Billing

NDC Package Code
47682-080-13
Package Description
250 PACKET in 1 BOX, UNIT-DOSE / 2 TABLET, FILM COATED in 1 PACKET
Product Code
47682-080
11-Digit Billing Format
47682008013

Clinical Specifications

Proprietary Name
Otis Clapp Ultraprin
Dosage Form
-

Regulatory & Marketing

Labeler Name
Unifirst First Aid Corporation
FDA Application #
ANDA071333
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
12-30-2008
End Marketing Date
11-01-2013
Listing Expiration
11-01-2013
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (47682-080). Click a package code to view its specific billing and regulatory data.

47682-080-99
2 TABLET, FILM COATED in 1 PACKET

* 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 47682-080-13 identifies a specific commercial package of 250 packet in 1 box, unit-dose / 2 tablet, film coated in 1 packet of Otis Clapp Ultraprin, labeled by Unifirst First Aid Corporation. 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 Unifirst First Aid Corporation on December 30, 2008. The current certification is valid through November 01, 2013.

How is this Unifirst First Aid Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 47682008013. 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)
47682-080-13
11-Digit CMS (5-4-2)
47682-0080-13

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