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
68462-393-01	68462-393	HUMAN PRESCRIPTION DRUG	raloxifene hydrochloride	raloxifene hydrochloride	TABLET, FILM COATED	ORAL	20160322	N/A	ANDA	ANDA204491	Glenmark Pharmaceuticals Inc., USA	RALOXIFENE HYDROCHLORIDE	60 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-393-01)
68462-393-10	68462-393	HUMAN PRESCRIPTION DRUG	raloxifene hydrochloride	raloxifene hydrochloride	TABLET, FILM COATED	ORAL	20160322	N/A	ANDA	ANDA204491	Glenmark Pharmaceuticals Inc., USA	RALOXIFENE HYDROCHLORIDE	60 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68462-393-10)
68462-393-23	68462-393	HUMAN PRESCRIPTION DRUG	raloxifene hydrochloride	raloxifene hydrochloride	TABLET, FILM COATED	ORAL	20160322	N/A	ANDA	ANDA204491	Glenmark Pharmaceuticals Inc., USA	RALOXIFENE HYDROCHLORIDE	60 mg/1	2000 TABLET, FILM COATED in 1 BOTTLE (68462-393-23)
68462-393-30	68462-393	HUMAN PRESCRIPTION DRUG	raloxifene hydrochloride	raloxifene hydrochloride	TABLET, FILM COATED	ORAL	20160322	N/A	ANDA	ANDA204491	Glenmark Pharmaceuticals Inc., USA	RALOXIFENE HYDROCHLORIDE	60 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68462-393-30)
68462-393-90	68462-393	HUMAN PRESCRIPTION DRUG	raloxifene hydrochloride	raloxifene hydrochloride	TABLET, FILM COATED	ORAL	20160322	N/A	ANDA	ANDA204491	Glenmark Pharmaceuticals Inc., USA	RALOXIFENE HYDROCHLORIDE	60 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68462-393-90)