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
71209-082-01	71209-082	HUMAN PRESCRIPTION DRUG	Raloxifene hydrochloride	Raloxifene hydrochloride	TABLET, COATED	ORAL	20171230	N/A	ANDA	ANDA211324	Cadila Pharmaceuticals Limited	RALOXIFENE HYDROCHLORIDE	60 mg/1	30 TABLET, COATED in 1 BOTTLE (71209-082-01)
71209-082-05	71209-082	HUMAN PRESCRIPTION DRUG	Raloxifene hydrochloride	Raloxifene hydrochloride	TABLET, COATED	ORAL	20171230	N/A	ANDA	ANDA211324	Cadila Pharmaceuticals Limited	RALOXIFENE HYDROCHLORIDE	60 mg/1	100 TABLET, COATED in 1 BOTTLE (71209-082-05)
71209-082-11	71209-082	HUMAN PRESCRIPTION DRUG	Raloxifene hydrochloride	Raloxifene hydrochloride	TABLET, COATED	ORAL	20211213	N/A	ANDA	ANDA211324	Cadila Pharmaceuticals Limited	RALOXIFENE HYDROCHLORIDE	60 mg/1	1000 TABLET, COATED in 1 BOTTLE (71209-082-11)
71209-082-13	71209-082	HUMAN PRESCRIPTION DRUG	Raloxifene hydrochloride	Raloxifene hydrochloride	TABLET, COATED	ORAL	20171230	N/A	ANDA	ANDA211324	Cadila Pharmaceuticals Limited	RALOXIFENE HYDROCHLORIDE	60 mg/1	2000 TABLET, COATED in 1 BOTTLE (71209-082-13)
72162-2418-0	72162-2418	HUMAN PRESCRIPTION DRUG	Raloxifene hydrochloride	Raloxifene hydrochloride	TABLET, COATED	ORAL	20241031	N/A	ANDA	ANDA211324	Bryant Ranch Prepack	RALOXIFENE HYDROCHLORIDE	60 mg/1	1000 TABLET, COATED in 1 BOTTLE (72162-2418-0)
72162-2418-1	72162-2418	HUMAN PRESCRIPTION DRUG	Raloxifene hydrochloride	Raloxifene hydrochloride	TABLET, COATED	ORAL	20241031	N/A	ANDA	ANDA211324	Bryant Ranch Prepack	RALOXIFENE HYDROCHLORIDE	60 mg/1	100 TABLET, COATED in 1 BOTTLE (72162-2418-1)
72162-2418-3	72162-2418	HUMAN PRESCRIPTION DRUG	Raloxifene hydrochloride	Raloxifene hydrochloride	TABLET, COATED	ORAL	20241031	N/A	ANDA	ANDA211324	Bryant Ranch Prepack	RALOXIFENE HYDROCHLORIDE	60 mg/1	30 TABLET, COATED in 1 BOTTLE (72162-2418-3)
72241-010-05	72241-010	HUMAN PRESCRIPTION DRUG	Raloxifene hydrochloride	Raloxifene hydrochloride	TABLET, COATED	ORAL	20171230	N/A	ANDA	ANDA211324	Modavar Pharmaceuticals LLC	RALOXIFENE HYDROCHLORIDE	60 mg/1	100 TABLET, COATED in 1 BOTTLE (72241-010-05)
72241-010-11	72241-010	HUMAN PRESCRIPTION DRUG	Raloxifene hydrochloride	Raloxifene hydrochloride	TABLET, COATED	ORAL	20171230	N/A	ANDA	ANDA211324	Modavar Pharmaceuticals LLC	RALOXIFENE HYDROCHLORIDE	60 mg/1	1000 TABLET, COATED in 1 BOTTLE (72241-010-11)
72241-010-13	72241-010	HUMAN PRESCRIPTION DRUG	Raloxifene hydrochloride	Raloxifene hydrochloride	TABLET, COATED	ORAL	20171230	N/A	ANDA	ANDA211324	Modavar Pharmaceuticals LLC	RALOXIFENE HYDROCHLORIDE	60 mg/1	2000 TABLET, COATED in 1 BOTTLE (72241-010-13)
72241-010-22	72241-010	HUMAN PRESCRIPTION DRUG	Raloxifene hydrochloride	Raloxifene hydrochloride	TABLET, COATED	ORAL	20171230	N/A	ANDA	ANDA211324	Modavar Pharmaceuticals LLC	RALOXIFENE HYDROCHLORIDE	60 mg/1	30 TABLET, COATED in 1 BOTTLE (72241-010-22)
50090-6177-1	50090-6177	HUMAN PRESCRIPTION DRUG	Raloxifene hydrochloride	Raloxifene hydrochloride	TABLET, COATED	ORAL	20221018	N/A	ANDA	ANDA211324	A-S Medication Solutions	RALOXIFENE HYDROCHLORIDE	60 mg/1	90 TABLET, COATED in 1 BOTTLE (50090-6177-1)