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  5. NDC Package Code: 71699-202-28 Xcopri Titration Pack

NDC Package 71699-202-28 Xcopri Titration Pack

Cenobamate Kit Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
71699-202-28
Package Description:
1 KIT in 1 CARTON * 1 TABLET, FILM COATED in 1 BLISTER PACK * 1 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
71699-202
Proprietary Name:
Xcopri Titration Pack
Non-Proprietary Name:
Cenobamate
Usage Information:
XCOPRI is indicated for the treatment of partial-onset seizures in adult patients.
11-Digit NDC Billing Format:
71699020228
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
  • RxCUI: 2265695 - cenobamate 50 MG Oral Tablet
  • RxCUI: 2265701 - XCOPRI 50 MG Oral Tablet
  • RxCUI: 2265701 - cenobamate 50 MG Oral Tablet [Xcopri]
  • RxCUI: 2265701 - Xcopri 50 MG Oral Tablet
  • RxCUI: 2283503 - cenobamate 100 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Sk Life Science, Inc.
    Dosage Form:
    Kit - A packaged collection of related material.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Sample Package:
    No
    FDA Application Number:
    NDA212839
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    03-12-2020
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Frequently Asked Questions

    What is NDC 71699-202-28?

    The NDC Packaged Code 71699-202-28 is assigned to a package of 1 kit in 1 carton * 1 tablet, film coated in 1 blister pack * 1 tablet, film coated in 1 blister pack of Xcopri Titration Pack, a human prescription drug labeled by Sk Life Science, Inc.. The product's dosage form is kit and is administered via oral form.

    Is NDC 71699-202 included in the NDC Directory?

    Yes, Xcopri Titration Pack with product code 71699-202 is active and included in the NDC Directory. The product was first marketed by Sk Life Science, Inc. on March 12, 2020 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 71699-202-28?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units.

    What is the 11-digit format for NDC 71699-202-28?

    The 11-digit format is 71699020228. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-271699-202-285-4-271699-0202-28