Mckesson Ibuprofen 200 Mg Tablet, Coated
NDC Package 68599-8051-4

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Mckesson Ibuprofen 200 Mg (ibuprofen) tablets is ibuprofen is used to help relieve mild to moderate pain. This formulation utilizes a tablet, coated delivery system. Marketed by Mckesson Medical-surgical, this product is identified by NDC 68599-8051 and is authorized under FDA application ANDA079174.

Identification & Billing

NDC Package Code
68599-8051-4
Package Description
200 PACKET in 1 BOX / 2 TABLET, COATED in 1 PACKET
Product Code
11-Digit Billing Format
68599805104
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Mckesson Ibuprofen 200 Mg
Non-Proprietary Name
Ibuprofen
Substance Name
Ibuprofen
Dosage Form
Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
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
Mckesson Medical-surgical
Product Type
Human Otc Drug
FDA Application #
ANDA079174
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
09-01-2021
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 68599-8051-4 identifies a specific commercial package of 200 packet in 1 box / 2 tablet, coated in 1 packet of Mckesson Ibuprofen 200 Mg, a human over the counter drug labeled by Mckesson Medical-surgical. This tablet, 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 Mckesson Medical-surgical on September 01, 2021. 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 Mckesson Medical-surgical product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 68599805104. 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 (5-4-1)
68599-8051-4
11-Digit CMS (5-4-2)
68599-8051-04

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