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
42543-408-01	42543-408	HUMAN PRESCRIPTION DRUG	POTASSIUM CITRATE EXTENDED RELEASE	POTASSIUM CITRATE	TABLET	ORAL	20171101	N/A	ANDA	ANDA206813	Strides Pharma Inc.	POTASSIUM CITRATE	15 meq/1	100 TABLET in 1 BOTTLE (42543-408-01)
42543-406-01	42543-406	HUMAN PRESCRIPTION DRUG	POTASSIUM CITRATE EXTENDED RELEASE	POTASSIUM CITRATE	TABLET	ORAL	20171101	N/A	ANDA	ANDA206813	Strides Pharma Inc.	POTASSIUM CITRATE	5 meq/1	100 TABLET in 1 BOTTLE (42543-406-01)
42543-407-01	42543-407	HUMAN PRESCRIPTION DRUG	POTASSIUM CITRATE EXTENDED RELEASE	POTASSIUM CITRATE	TABLET	ORAL	20171101	N/A	ANDA	ANDA206813	Strides Pharma Inc.	POTASSIUM CITRATE	10 meq/1	100 TABLET in 1 BOTTLE (42543-407-01)
71335-1706-1	71335-1706	HUMAN PRESCRIPTION DRUG	POTASSIUM CITRATE EXTENDED RELEASE	POTASSIUM CITRATE	TABLET	ORAL	20200910	N/A	ANDA	ANDA206813	Bryant Ranch Prepack	POTASSIUM CITRATE	10 meq/1	30 TABLET in 1 BOTTLE (71335-1706-1)