| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 51167-700-02 | 51167-700 | HUMAN PRESCRIPTION DRUG | ORKAMBI | lumacaftor and ivacaftor | TABLET, FILM COATED | ORAL | 20160928 | N/A | NDA | NDA206038 | Vertex Pharmaceuticals Incorporated | IVACAFTOR; LUMACAFTOR | 125 mg/1; 100 mg/1 | 4 CARTON in 1 BOX (51167-700-02) / 7 BLISTER PACK in 1 CARTON / 4 TABLET, FILM COATED in 1 BLISTER PACK |
| 51167-809-01 | 51167-809 | HUMAN PRESCRIPTION DRUG | ORKAMBI | lumacaftor and ivacaftor | TABLET, FILM COATED | ORAL | 20150702 | N/A | NDA | NDA206038 | Vertex Pharmaceuticals Incorporated | IVACAFTOR; LUMACAFTOR | 125 mg/1; 200 mg/1 | 4 CARTON in 1 BOX (51167-809-01) / 7 BLISTER PACK in 1 CARTON / 4 TABLET, FILM COATED in 1 BLISTER PACK |