Otis Clapp Ultraprin
NDC Package 47682-702-13

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.

Otis Clapp Ultraprin is ■ do not use more than directed■ the smallest effective dose should be used■ do not take longer than 10 days, unless directed by a doctor (see Warnings)Adults and children:(12 years and older)Take 1 tablet every 4 to 6 hours while symptoms persist. Marketed by Unifirst First Aid Corporation, this product is identified by NDC 47682-702 and is authorized under FDA application ANDA079174.

Identification & Billing

NDC Package Code
47682-702-13
Package Description
250 PACKET in 1 BOX / 2 TABLET, COATED in 1 PACKET (47682-702-99)
Product Code
47682-702
11-Digit Billing Format
47682070213
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Otis Clapp Ultraprin
Dosage Form
-
Usage Information
■ do not use more than directed■ the smallest effective dose should be used■ do not take longer than 10 days, unless directed by a doctor (see Warnings)Adults and children:(12 years and older)Take 1 tablet every 4 to 6 hours while symptoms persist. If pain or fever does not respond to 1 tablet, 2 tablets may be used. Do not exceed 6 tablets in 24 hours, unless directed by a doctor. Children under 12 years:Do not give to children under 12 years of age.

Regulatory & Marketing

Labeler Name
Unifirst First Aid Corporation
FDA Application #
ANDA079174
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
11-17-2014
End Marketing Date
04-03-2017
Listing Expiration
04-03-2017
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 47682-702-13 identifies a specific commercial package of 250 packet in 1 box / 2 tablet, coated in 1 packet (47682-702-99) 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 November 17, 2014. The current certification is valid through April 03, 2017.

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: 47682070213. 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)
47682-702-13
11-Digit CMS (5-4-2)
47682-0702-13

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