NDC 50474-808

Neupro

Rotigotine

Neupro is a Kit in the Human Prescription Drug category. It is labeled and distributed by Ucb, Inc.. The primary component is .

Product ID50474-808_35c1c048-bc3d-4579-b73b-6e77389e81f5
NDC50474-808
Product TypeHuman Prescription Drug
Proprietary NameNeupro
Generic NameRotigotine
Dosage FormKit
Marketing Start Date2012-04-02
Marketing CategoryNDA / NDA
Application NumberNDA021829
Labeler NameUCB, Inc.
Active Ingredient Strength0
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 50474-808-11

2 BOX in 1 KIT (50474-808-11) > 1 KIT in 1 BOX * 7 POUCH in 1 BOX > 1 PATCH in 1 POUCH > 24 h in 1 PATCH * 7 POUCH in 1 BOX > 1 PATCH in 1 POUCH > 24 h in 1 PATCH
Marketing Start Date2012-04-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50474-808-11 [50474080811]

Neupro KIT
Marketing CategoryNDA
Application NumberNDA021829
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-04-02

Drug Details

OpenFDA Data

SPL SET ID:939e28c5-f3a9-42c0-9a2d-8d471d82a6e0
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 722256
  • 1251914
  • 724142
  • 1251922
  • 722253
  • 1251912
  • 722295
  • 722279
  • 1251918
  • 1251916
  • 1360633
  • 1251920
  • 724156
  • 1360632
  • NDC Crossover Matching brand name "Neupro" or generic name "Rotigotine"

    NDCBrand NameGeneric Name
    50474-801Neuprorotigotine
    50474-802Neuprorotigotine
    50474-803Neuprorotigotine
    50474-804Neuprorotigotine
    50474-805Neuprorotigotine
    50474-806Neuprorotigotine
    50474-808Neuprorotigotine

    Trademark Results [Neupro]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    NEUPRO
    NEUPRO
    79069118 3763462 Live/Registered
    UCB Pharma GmbH
    2009-02-14
    NEUPRO
    NEUPRO
    76492893 2836118 Live/Registered
    UCB PHARMA GMBH
    2003-02-25
    NEUPRO
    NEUPRO
    75936415 not registered Dead/Abandoned
    Schwarz Pharma AG
    2000-03-06

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