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）

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
65162-057-03	65162-057	HUMAN PRESCRIPTION DRUG	Raloxifene Hydrochloride	Raloxifene Hydrochloride	TABLET, FILM COATED	ORAL	20160120	N/A	ANDA	ANDA208206	Amneal Pharmaceuticals LLC	RALOXIFENE HYDROCHLORIDE	60 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65162-057-03)
65162-057-09	65162-057	HUMAN PRESCRIPTION DRUG	Raloxifene Hydrochloride	Raloxifene Hydrochloride	TABLET, FILM COATED	ORAL	20160120	N/A	ANDA	ANDA208206	Amneal Pharmaceuticals LLC	RALOXIFENE HYDROCHLORIDE	60 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65162-057-09)
65162-057-10	65162-057	HUMAN PRESCRIPTION DRUG	Raloxifene Hydrochloride	Raloxifene Hydrochloride	TABLET, FILM COATED	ORAL	20160120	N/A	ANDA	ANDA208206	Amneal Pharmaceuticals LLC	RALOXIFENE HYDROCHLORIDE	60 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65162-057-10)
65162-057-11	65162-057	HUMAN PRESCRIPTION DRUG	Raloxifene Hydrochloride	Raloxifene Hydrochloride	TABLET, FILM COATED	ORAL	20160120	N/A	ANDA	ANDA208206	Amneal Pharmaceuticals LLC	RALOXIFENE HYDROCHLORIDE	60 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65162-057-11)
65162-057-33	65162-057	HUMAN PRESCRIPTION DRUG	Raloxifene Hydrochloride	Raloxifene Hydrochloride	TABLET, FILM COATED	ORAL	20160120	N/A	ANDA	ANDA208206	Amneal Pharmaceuticals LLC	RALOXIFENE HYDROCHLORIDE	60 mg/1	2000 TABLET, FILM COATED in 1 BOTTLE (65162-057-33)
65162-057-50	65162-057	HUMAN PRESCRIPTION DRUG	Raloxifene Hydrochloride	Raloxifene Hydrochloride	TABLET, FILM COATED	ORAL	20160120	N/A	ANDA	ANDA208206	Amneal Pharmaceuticals LLC	RALOXIFENE HYDROCHLORIDE	60 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65162-057-50)
50268-694-15	50268-694	HUMAN PRESCRIPTION DRUG	Raloxifene Hydrochloride	Raloxifene Hydrochloride	TABLET, FILM COATED	ORAL	20180627	N/A	ANDA	ANDA208206	AvPAK	RALOXIFENE HYDROCHLORIDE	60 mg/1	50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-694-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-694-11)