| NDC包装代码 | 产品NDC | 产品类型 | 商品名 | 通用名 | 剂型 | 给药途径 | 上市日期 | 结束日期 | 市场类别 | 申请号 | 标签持有者 | 活性成分 | 规格 | 包装描述 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 59676-575-30 | 59676-575 | HUMAN PRESCRIPTION DRUG | PREZCOBIX | DARUNAVIR ETHANOLATE and COBICISTAT | TABLET, FILM COATED | ORAL | 20150131 | N/A | NDA | NDA205395 | Janssen Products LP | COBICISTAT; DARUNAVIR ETHANOLATE | 150 mg/1; 800 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (59676-575-30) |
| 50090-1723-0 | 50090-1723 | HUMAN PRESCRIPTION DRUG | PREZCOBIX | DARUNAVIR ETHANOLATE and COBICISTAT | TABLET, FILM COATED | ORAL | 20150304 | N/A | NDA | NDA205395 | A-S Medication Solutions | COBICISTAT; DARUNAVIR ETHANOLATE | 150 mg/1; 800 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-1723-0) |