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  5. NDC Package Code: 50474-801-03 Neupro

NDC Package 50474-801-03 Neupro

Rotigotine Patch, Extended Release Transdermal - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
50474-801-03
Package Description:
30 POUCH in 1 CARTON / 1 PATCH in 1 POUCH / 24 h in 1 PATCH
Product Code:
50474-801
Proprietary Name:
Neupro
Non-Proprietary Name:
Rotigotine
Substance Name:
Rotigotine
Usage Information:
Rotigotine is used alone or with other medications to treat Parkinson's disease. It can improve your ability to move and decrease shakiness (tremor), stiffness, slowed movement, and unsteadiness. Rotigotine is also used to treat restless legs syndrome (RLS). Rotigotine is a dopamine agonist that works by helping to restore the balance of a certain natural substance (dopamine) in the brain.
11-Digit NDC Billing Format:
50474080103
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1251912 - rotigotine 1 MG/Day 24HR Transdermal System
  • RxCUI: 1251912 - 24 HR rotigotine 0.0417 MG/HR Transdermal System
  • RxCUI: 1251912 - rotigotine 0.0417 MG/HR 24 HR Transdermal Patch
  • RxCUI: 1251912 - rotigotine 1 MG/Day 24 HR Transdermal Patch
  • RxCUI: 1251914 - Neupro 1 MG/Day 24HR Transdermal System
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Ucb, Inc.
    Dosage Form:
    Patch, Extended Release - A drug delivery system in the form of a patch that releases the drug in such a manner that a reduction in dosing frequency compared to that drug presented as a conventional dosage form (e.g., a solution or a prompt drug-releasing, conventional solid dosage form).
    Administration Route(s):
  • Transdermal - Administration through the dermal layer of the skin to the systemic circulation by diffusion.
    • Active Ingredient(s):
  • ROTIGOTINE 1 mg/24h
    • Sample Package:
    No
    FDA Application Number:
    NDA021829
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    04-02-2012
    Listing Expiration Date:
    12-31-2024
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    50474-801-177 POUCH in 1 CARTON / 1 PATCH in 1 POUCH / 24 h in 1 PATCH

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50474-801-03?

    The NDC Packaged Code 50474-801-03 is assigned to a package of 30 pouch in 1 carton / 1 patch in 1 pouch / 24 h in 1 patch of Neupro, a human prescription drug labeled by Ucb, Inc.. The product's dosage form is patch, extended release and is administered via transdermal form.

    Is NDC 50474-801 included in the NDC Directory?

    Yes, Neupro with product code 50474-801 is active and included in the NDC Directory. The product was first marketed by Ucb, Inc. on April 02, 2012 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 50474-801-03?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 1.

    What is the 11-digit format for NDC 50474-801-03?

    The 11-digit format is 50474080103. 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
    5-3-250474-801-035-4-250474-0801-03