50474-808 : Neupro Kit


NDC: 50474-808
Labeler: Ucb, Inc.
Product Type: Human Prescription Drug
Drug Name:  Neupro
Dosage Form: Kit
Application #: NDA021829
Rev. Date: 


NDC Package Codes:

  • 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

Active Ingredients:

  • Rotigotine

Related Products:

Based on records with the same trade name.
  • 50474-801 Neupro 1 mg/24h Transdermal Patch, Extended Release by Ucb, Inc.
  • 50474-802 Neupro 2 mg/24h Transdermal Patch, Extended Release by Ucb, Inc.
  • 50474-803 Neupro 3 mg/24h Transdermal Patch, Extended Release by Ucb, Inc.
  • 50474-804 Neupro 4 mg/24h Transdermal Patch, Extended Release by Ucb, Inc.
  • 50474-805 Neupro 6 mg/24h Transdermal Patch, Extended Release by Ucb, Inc.
  • 50474-806 Neupro 8 mg/24h Transdermal Patch, Extended Release by Ucb, Inc.

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 50474-808 QR Code

< Prev: 50474-806Next: 50474-870 >




Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.