Medi-first Ibuprofen
NDC Package 47682-708-33

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.

Medi-first Ibuprofen is a . Marketed by Unifirst First Aid Corporation, this product is identified by NDC 47682-708 and is authorized under FDA application ANDA079174.

Identification & Billing

NDC Package Code
47682-708-33
Package Description
50 PACKET in 1 BOX, UNIT-DOSE / 2 TABLET, COATED in 1 PACKET
Product Code
47682-708
11-Digit Billing Format
47682070833
RxNorm Crosswalk
  • RxCUI: 1367204 - acetaminophen 325 MG / dextromethorphan HBr 15 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1367204 - acetaminophen 325 MG / dextromethorphan hydrobromide 15 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1367204 - APAP 325 MG / dextromethorphan hydrobromide 15 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 198440 - acetaminophen 500 MG Oral Tablet
  • RxCUI: 198440 - APAP 500 MG Oral Tablet

Clinical Specifications

Proprietary Name
Medi-first Ibuprofen
Dosage Form
-

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
01-26-2017
End Marketing Date
10-26-2018
Listing Expiration
10-26-2018
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 (47682-708). Click a package code to view its specific billing and regulatory data.

47682-708-13
250 PACKET in 1 BOX, UNIT-DOSE / 2 TABLET, COATED in 1 PACKET (47682-708-99)
47682-708-30
4 PACKET in 1 BOX, UNIT-DOSE / 2 TABLET, COATED in 1 PACKET
47682-708-48
125 PACKET in 1 BOX, UNIT-DOSE / 2 TABLET, 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 47682-708-33 identifies a specific commercial package of 50 packet in 1 box, unit-dose / 2 tablet, coated in 1 packet of Medi-first Ibuprofen, 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 January 26, 2017. The current certification is valid through October 26, 2018.

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: 47682070833. 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)
47682-708-33
11-Digit CMS (5-4-2)
47682-0708-33

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