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
59651-299-60	59651-299	HUMAN PRESCRIPTION DRUG	Tamoxifen Citrate	Tamoxifen Citrate	TABLET, FILM COATED	ORAL	20200814	N/A	ANDA	ANDA213358	Aurobindo Pharma Limited	TAMOXIFEN CITRATE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (59651-299-60)
72162-2209-3	72162-2209	HUMAN PRESCRIPTION DRUG	Tamoxifen Citrate	Tamoxifen Citrate	TABLET, FILM COATED	ORAL	20240105	N/A	ANDA	ANDA213358	Bryant Ranch Prepack	TAMOXIFEN CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72162-2209-3)
59651-300-30	59651-300	HUMAN PRESCRIPTION DRUG	Tamoxifen Citrate	Tamoxifen Citrate	TABLET, FILM COATED	ORAL	20200814	N/A	ANDA	ANDA213358	Aurobindo Pharma Limited	TAMOXIFEN CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (59651-300-30)
59651-300-90	59651-300	HUMAN PRESCRIPTION DRUG	Tamoxifen Citrate	Tamoxifen Citrate	TABLET, FILM COATED	ORAL	20200814	N/A	ANDA	ANDA213358	Aurobindo Pharma Limited	TAMOXIFEN CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (59651-300-90)
72162-2208-6	72162-2208	HUMAN PRESCRIPTION DRUG	Tamoxifen Citrate	Tamoxifen Citrate	TABLET, FILM COATED	ORAL	20240105	N/A	ANDA	ANDA213358	Bryant Ranch Prepack	TAMOXIFEN CITRATE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72162-2208-6)