NDC 0131-2470

Vimpat

Lacosamide

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

• Product ID: 0131-2470_36e26c97-31c2-4c80-9bc0-ab039a0349a0
• NDC: 0131-2470
• Product Type: Human Prescription Drug
• Proprietary Name: Vimpat
• Generic Name: Lacosamide
• Dosage Form: Kit
• Marketing Start Date: 2009-05-26
• Marketing Category: NDA / NDA
• Application Number: NDA022253
• Labeler Name: UCB, Inc.
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 0131-2470-99

1 BLISTER PACK in 1 CARTON (0131-2470-99) > 1 KIT in 1 BLISTER PACK

• Marketing Start Date: 2009-05-26
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0131-2470-99 [00131247099]

Vimpat KIT

• Marketing Category: NDA
• Application Number: NDA022253
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-05-26

Drug Details

OpenFDA Data

• SPL SET ID: 9e79b42c-38a3-4b2c-a196-a5a1948250e2
• Manufacturer:
  • UCB, Inc.
• UNII:
  • 563KS2PQY5
• RxNorm Concept Unique ID - RxCUI:
  • 809984
  • 809992
  • 809987
  • 809996
  • 809994
  • 809974
  • 809998
  • 993856
  • 810002
  • 810000
  • 809990
  • 881272
  • 881271
  • 995156
• UPC Code:
  • 0301315410714
  • 0301315410707
  • 0301312477352
  • 0301312478359
  • 0301312479356
  • 0301312480352

NDC Crossover Matching brand name "Vimpat" or generic name "Lacosamide"

NDC	Brand Name	Generic Name
0131-1810	Vimpat	lacosamide
0131-2470	Vimpat	lacosamide
0131-2477	Vimpat	lacosamide
0131-2478	Vimpat	lacosamide
0131-2479	Vimpat	lacosamide
70518-0257	Vimpat	Vimpat
0131-5410	Vimpat	Vimpat
0131-2480	Vimpat	Vimpat
70166-617	Vimpat	Vimpat
0121-0992	Lacosamide	Lacosamide
0121-1984	Lacosamide	Lacosamide
0121-2976	Lacosamide	Lacosamide
0121-3968	Lacosamide	Lacosamide