ZEPATIER is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Merck Sharp & Dohme Corp.. The primary component is Elbasvir; Grazoprevir Anhydrous.
| Product ID | 0006-3074_1496b16e-fbbf-46e5-b2e8-e983026663be | 
| NDC | 0006-3074 | 
| Product Type | Human Prescription Drug | 
| Proprietary Name | ZEPATIER | 
| Generic Name | Elbasvir And Grazoprevir | 
| Dosage Form | Tablet, Film Coated | 
| Route of Administration | ORAL | 
| Marketing Start Date | 2016-01-28 | 
| Marketing Category | NDA / NDA | 
| Application Number | NDA208261 | 
| Labeler Name | Merck Sharp & Dohme Corp. | 
| Substance Name | ELBASVIR; GRAZOPREVIR ANHYDROUS | 
| Active Ingredient Strength | 50 mg/1; mg/1 | 
| Pharm Classes | Hepatitis C Virus NS5A Inhibitor [EPC],Breast Cancer Resistance Protein Inhibitors [MoA],HCV NS3/4A Protease Inhibitors [MoA],Hepatitis C Virus NS3/4A Protease Inhibitor [EPC],Breast Cancer Resistance Protein Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA] | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2021-12-31 | 
| Marketing Start Date | 2016-01-28 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | NDA | 
| Application Number | NDA208261 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2016-01-28 | 
| Marketing Category | NDA | 
| Application Number | NDA208261 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2016-01-28 | 
| Ingredient | Strength | 
|---|---|
| ELBASVIR | 50 mg/1 | 
| SPL SET ID: | 164dc02a-9180-426a-b8b5-04ab39d2bbd4 | 
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  ZEPATIER  86336186  4937479 Live/Registered | Merck Sharp & Dohme Corp. 2014-07-14 |