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
71335-1715-1	71335-1715	HUMAN PRESCRIPTION DRUG	Raloxifene Hydrochloride	Raloxifene Hydrochloride	TABLET, FILM COATED	ORAL	20201002	N/A	ANDA	ANDA078193	Bryant Ranch Prepack	RALOXIFENE HYDROCHLORIDE	60 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1715-1)
71335-1715-2	71335-1715	HUMAN PRESCRIPTION DRUG	Raloxifene Hydrochloride	Raloxifene Hydrochloride	TABLET, FILM COATED	ORAL	20211229	N/A	ANDA	ANDA078193	Bryant Ranch Prepack	RALOXIFENE HYDROCHLORIDE	60 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1715-2)
0093-7290-01	0093-7290	HUMAN PRESCRIPTION DRUG	Raloxifene Hydrochloride	Raloxifene Hydrochloride	TABLET, FILM COATED	ORAL	20140328	N/A	ANDA	ANDA078193	Teva Pharmaceuticals USA, Inc.	RALOXIFENE HYDROCHLORIDE	60 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0093-7290-01)
0093-7290-56	0093-7290	HUMAN PRESCRIPTION DRUG	Raloxifene Hydrochloride	Raloxifene Hydrochloride	TABLET, FILM COATED	ORAL	20140328	N/A	ANDA	ANDA078193	Teva Pharmaceuticals USA, Inc.	RALOXIFENE HYDROCHLORIDE	60 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-7290-56)