ZONTIVITY is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Aralez Pharmaceuticals Us Inc.. The primary component is Vorapaxar Sulfate.
Product ID | 70347-208_3ae89838-2877-4ec7-a705-b0821957a1d4 |
NDC | 70347-208 |
Product Type | Human Prescription Drug |
Proprietary Name | ZONTIVITY |
Generic Name | Vorapaxar |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 2014-05-08 |
Marketing Category | NDA / NDA |
Application Number | NDA204886 |
Labeler Name | Aralez Pharmaceuticals Us Inc. |
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 | 2020-12-31 |
Marketing Start Date | 2017-07-06 |
NDC Exclude Flag | N |
Sample Package? | Y |
Marketing Category | NDA |
Application Number | NDA204886 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2017-04-01 |
Marketing Category | NDA |
Application Number | NDA204886 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2017-04-01 |
Marketing Category | NDA |
Application Number | NDA204886 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2017-07-06 |
Ingredient | Strength |
---|---|
VORAPAXAR SULFATE | 2.08 mg/1 |
SPL SET ID: | f001f406-8cf1-40a4-bbf5-1775fe020122 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
66992-208 | ZONTIVITY | vorapaxar |
70347-208 | ZONTIVITY | vorapaxar |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ZONTIVITY 86164928 not registered Dead/Abandoned |
Merck Sharp & Dohme Corp. 2014-01-14 |
ZONTIVITY 85307417 4628973 Live/Registered |
ARALEZ PHARMACEUTICALS TRADING DESIGNATED ACTIVITY COMPANY 2011-04-28 |