| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 50419-489-01 | 50419-489 | HUMAN PRESCRIPTION DRUG | Nexavar | sorafenib | TABLET, FILM COATED | ORAL | 20231002 | N/A | NDA | NDA021923 | Bayer HealthCare Pharmaceuticals Inc. | SORAFENIB | 200 mg/1 | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-489-01) |
| 50419-488-58 | 50419-488 | HUMAN PRESCRIPTION DRUG | Nexavar | sorafenib | TABLET, FILM COATED | ORAL | 20051220 | N/A | NDA | NDA021923 | Bayer HealthCare Pharmaceuticals Inc. | SORAFENIB | 200 mg/1 | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-488-58) |