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
17856-0831-1	17856-0831	HUMAN PRESCRIPTION DRUG	Sodium Polystyrene Sulfonate	Sodium Polystyrene Sulfonate	POWDER, FOR SUSPENSION	ORAL; RECTAL	20240529	N/A	ANDA	ANDA090313	ATLANTIC BIOLOGICALS CORP.	SODIUM POLYSTYRENE SULFONATE	4.1 meq/g	50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0831-1) / 15 g in 1 CUP, UNIT-DOSE
17856-0831-2	17856-0831	HUMAN PRESCRIPTION DRUG	Sodium Polystyrene Sulfonate	Sodium Polystyrene Sulfonate	POWDER, FOR SUSPENSION	ORAL; RECTAL	20240529	N/A	ANDA	ANDA090313	ATLANTIC BIOLOGICALS CORP.	SODIUM POLYSTYRENE SULFONATE	4.1 meq/g	50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0831-2) / 30 g in 1 CUP, UNIT-DOSE
63629-2031-1	63629-2031	HUMAN PRESCRIPTION DRUG	Sodium Polystyrene Sulfonate	Sodium Polystyrene Sulfonate	POWDER, FOR SUSPENSION	ORAL; RECTAL	20220308	N/A	ANDA	ANDA090313	Bryant Ranch Prepack	SODIUM POLYSTYRENE SULFONATE	4.1 meq/g	453.6 g in 1 JAR (63629-2031-1)