NDC 66992-208

ZONTIVITY

Vorapaxar

ZONTIVITY is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Wraser Pharmaceuticals, Llc. The primary component is Vorapaxar Sulfate.

• Product ID: 66992-208_e946b6c2-23db-0d65-e053-2a95a90acd48
• NDC: 66992-208
• Product Type: Human Prescription Drug
• Proprietary Name: ZONTIVITY
• Generic Name: Vorapaxar
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2022-09-21
• Marketing Category: NDA /
• Application Number: NDA204886
• Labeler Name: WraSer Pharmaceuticals, LLC
• Substance Name: VORAPAXAR SULFATE
• Active Ingredient Strength: 2 mg/1
• Pharm Classes: Protease-activated Receptor-1 Antagonist [EPC], Protease-activated Receptor-1 Antagonists [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 66992-208-30

30 TABLET, FILM COATED in 1 BOTTLE (66992-208-30)

• Marketing Start Date: 2022-09-21
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "ZONTIVITY" or generic name "Vorapaxar"

NDC	Brand Name	Generic Name
66992-208	ZONTIVITY	vorapaxar
70347-208	ZONTIVITY	vorapaxar