美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=NDA209115"
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
82154-0783-1 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)
69660-203-91 69660-203 HUMAN PRESCRIPTION DRUG Rubraca rucaparib TABLET, FILM COATED ORAL 20161219 20250731 NDA NDA209115 Clovis Oncology, Inc. RUCAPARIB CAMSYLATE 300 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (69660-203-91)
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)
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)
69660-202-91 69660-202 HUMAN PRESCRIPTION DRUG Rubraca rucaparib TABLET, FILM COATED ORAL 20170501 20250731 NDA NDA209115 Clovis Oncology, Inc. RUCAPARIB CAMSYLATE 250 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (69660-202-91)
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