Medi-first Ibuprofen Tablet, Film Coated
NDC Package 47682-608-48

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

Medi-first Ibuprofen (ibuprofen) tablets is ibuprofen is used to help relieve mild to moderate pain. This formulation utilizes a tablet, film coated delivery system. Marketed by Unifirst First Aid Corporation, this product is identified by NDC 47682-608 and is authorized under FDA application ANDA075010.

Identification & Billing

NDC Package Code
47682-608-48
Package Description
125 PACKET in 1 BOX / 2 TABLET, FILM COATED in 1 PACKET
Product Code
47682-608
11-Digit Billing Format
47682060848
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Medi-first Ibuprofen
Non-Proprietary Name
Ibuprofen
Substance Name
Ibuprofen
Dosage Form
Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
IBUPROFEN 200 mg/1
Pharmacologic Class
Usage Information
Ibuprofen is used to help relieve mild to moderate pain. When used with an opioid (such as morphine), it may be used to relieve moderate to severe pain. It is also used to reduce fever. Ibuprofen is known as a nonsteroidal anti-inflammatory drug (NSAID). It works by blocking your body's production of certain natural substances that cause inflammation. This effect helps to decrease swelling, pain, or fever.

Regulatory & Marketing

Labeler Name
Unifirst First Aid Corporation
Product Type
Human Otc Drug
FDA Application #
ANDA075010
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
02-01-2016
Listing Expiration
12-31-2026
Exclude Flag
N
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 (47682-608). Click a package code to view its specific billing and regulatory data.

47682-608-13
250 PACKET in 1 BOX / 2 TABLET, FILM COATED in 1 PACKET
47682-608-30
4 PACKET in 1 BOX / 2 TABLET, FILM COATED in 1 PACKET (47682-608-99)
47682-608-33
50 PACKET in 1 BOX / 2 TABLET, FILM COATED in 1 PACKET
47682-608-50
25 PACKET in 1 BOX / 2 TABLET, FILM COATED in 1 PACKET
47682-608-99
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 47682-608-48 identifies a specific commercial package of 125 packet in 1 box / 2 tablet, film coated in 1 packet of Medi-first Ibuprofen, a human over the counter drug labeled by Unifirst First Aid Corporation. This tablet, film coated is formulated for oral use and contains ibuprofen as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Unifirst First Aid Corporation on February 01, 2016. The current certification is valid through December 31, 2026.

What are the primary indications for this medication?

Ibuprofen is used to help relieve mild to moderate pain. When used with an opioid (such as morphine), it may be used to relieve moderate to severe pain. It is also used to reduce fever. Ibuprofen is known as a nonsteroidal anti-inflammatory drug (NSAID). It works by blocking your body's production of certain natural substances that cause inflammation. This effect helps to decrease swelling, pain, or fever.

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: 47682060848. 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)
47682-608-48
11-Digit CMS (5-4-2)
47682-0608-48

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