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 ID: 50474-808_35c1c048-bc3d-4579-b73b-6e77389e81f5
• NDC: 50474-808
• Product Type: Human Prescription Drug
• Proprietary Name: Neupro
• Generic Name: Rotigotine
• Dosage Form: Kit
• Marketing Start Date: 2012-04-02
• Marketing Category: NDA / NDA
• Application Number: NDA021829
• Labeler Name: UCB, Inc.
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

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 Date: 2012-04-02
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 50474-808-11 [50474080811]

Neupro KIT

• Marketing Category: NDA
• Application Number: NDA021829
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2012-04-02

Drug Details

OpenFDA Data

• SPL SET ID: 939e28c5-f3a9-42c0-9a2d-8d471d82a6e0
• Manufacturer:
  • UCB, Inc.
• UNII:
  • 87T4T8BO2E
• 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"

NDC	Brand Name	Generic Name
50474-801	Neupro	rotigotine
50474-802	Neupro	rotigotine
50474-803	Neupro	rotigotine
50474-804	Neupro	rotigotine
50474-805	Neupro	rotigotine
50474-806	Neupro	rotigotine
50474-808	Neupro	rotigotine