| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 82154-0785-1 | 82154-0785 | HUMAN PRESCRIPTION DRUG | Rubraca | rucaparib | TABLET, FILM COATED | ORAL | 20161219 | N/A | NDA | NDA209115 | pharmaand GmbH | RUCAPARIB CAMSYLATE | 300 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (82154-0785-1) |
| 82154-0783-1 | 82154-0783 | HUMAN PRESCRIPTION DRUG | Rubraca | rucaparib | TABLET, FILM COATED | ORAL | 20161219 | N/A | NDA | NDA209115 | pharmaand GmbH | RUCAPARIB CAMSYLATE | 200 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (82154-0783-1) |
| 82154-0784-1 | 82154-0784 | HUMAN PRESCRIPTION DRUG | Rubraca | rucaparib | TABLET, FILM COATED | ORAL | 20170501 | N/A | NDA | NDA209115 | pharmaand GmbH | RUCAPARIB CAMSYLATE | 250 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (82154-0784-1) |
| 69660-201-91 | 69660-201 | HUMAN PRESCRIPTION DRUG | Rubraca | rucaparib | TABLET, FILM COATED | ORAL | 20161219 | 20251231 | NDA | NDA209115 | Clovis Oncology, Inc. | RUCAPARIB CAMSYLATE | 200 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (69660-201-91) |