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
71610-472-30	71610-472	HUMAN PRESCRIPTION DRUG	CHLORTHALIDONE	CHLORTHALIDONE	TABLET	ORAL	20201009	N/A	ANDA	ANDA206904	Aphena Pharma Solutions - Tennessee, LLC	CHLORTHALIDONE	25 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (71610-472-30)
71610-472-45	71610-472	HUMAN PRESCRIPTION DRUG	CHLORTHALIDONE	CHLORTHALIDONE	TABLET	ORAL	20201009	N/A	ANDA	ANDA206904	Aphena Pharma Solutions - Tennessee, LLC	CHLORTHALIDONE	25 mg/1	45 TABLET in 1 BOTTLE, PLASTIC (71610-472-45)
71610-472-60	71610-472	HUMAN PRESCRIPTION DRUG	CHLORTHALIDONE	CHLORTHALIDONE	TABLET	ORAL	20201009	N/A	ANDA	ANDA206904	Aphena Pharma Solutions - Tennessee, LLC	CHLORTHALIDONE	25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (71610-472-60)
64980-303-01	64980-303	HUMAN PRESCRIPTION DRUG	CHLORTHALIDONE	CHLORTHALIDONE	TABLET	ORAL	20170517	20270131	ANDA	ANDA206904	Rising Pharma Holdings, Inc.	CHLORTHALIDONE	25 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (64980-303-01)
64980-303-10	64980-303	HUMAN PRESCRIPTION DRUG	CHLORTHALIDONE	CHLORTHALIDONE	TABLET	ORAL	20170517	20270131	ANDA	ANDA206904	Rising Pharma Holdings, Inc.	CHLORTHALIDONE	25 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (64980-303-10)
64980-304-01	64980-304	HUMAN PRESCRIPTION DRUG	CHLORTHALIDONE	CHLORTHALIDONE	TABLET	ORAL	20170517	20270131	ANDA	ANDA206904	Rising Pharma Holdings, Inc.	CHLORTHALIDONE	50 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (64980-304-01)