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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
50242-717-01 | 50242-717 | HUMAN PRESCRIPTION DRUG | Cotellic | COBIMETINIB | TABLET, FILM COATED | ORAL | 20151110 | N/A | NDA | NDA206192 | Genentech, Inc. | COBIMETINIB FUMARATE | 20 mg/1 | 63 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50242-717-01) |
50242-717-86 | 50242-717 | HUMAN PRESCRIPTION DRUG | Cotellic | COBIMETINIB | TABLET, FILM COATED | ORAL | 20151110 | N/A | NDA | NDA206192 | Genentech, Inc. | COBIMETINIB FUMARATE | 20 mg/1 | 63 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50242-717-86) |