Reus Nr
NDC Package 83663-003-02

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 inactivated by the FDA.

Reus Nr is adults and children 12 years of age and over: take 2 capsules not more often than every 3 to 4 hours. Marketed by Reus Polska Sp Z O O, this product is identified by NDC 83663-003.

Identification & Billing

NDC Package Code
83663-003-02
Package Description
80 BOTTLE in 1 BOTTLE / 80 BOTTLE in 1 BOTTLE / 80 CAPSULE in 1 BOTTLE (83663-003-01)
Product Code
83663-003
11-Digit Billing Format
83663000302

Clinical Specifications

Proprietary Name
Reus Nr
Dosage Form
-
Usage Information
Adults and children 12 years of age and over: take 2 capsules not more often than every 3 to 4 hours

Regulatory & Marketing

Labeler Name
Reus Polska Sp Z O O
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
07-20-2023
Listing Expiration
12-31-2024
Exclude Flag
I
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 83663-003-02 identifies a specific commercial package of 80 bottle in 1 bottle / 80 bottle in 1 bottle / 80 capsule in 1 bottle (83663-003-01) of Reus Nr, labeled by Reus Polska Sp Z O O. 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 Reus Polska Sp Z O O on July 20, 2023. The current certification is valid through December 31, 2024.

How is this Reus Polska Sp Z O O product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83663000302. 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)
83663-003-02
11-Digit CMS (5-4-2)
83663-0003-02

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