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
72189-462-30	72189-462	HUMAN PRESCRIPTION DRUG	Potassium Chloride ER	Potassium Chloride ER	TABLET, EXTENDED RELEASE	ORAL	20230417	N/A	ANDA	ANDA203562	Direct_Rx	POTASSIUM CHLORIDE	1500 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-462-30)
68462-471-05	68462-471	HUMAN PRESCRIPTION DRUG	potassium chloride	potassium chloride	TABLET, EXTENDED RELEASE	ORAL	20160726	N/A	ANDA	ANDA203562	Glenmark Pharmaceuticals Inc., USA	POTASSIUM CHLORIDE	750 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-471-05)
68462-472-01	68462-472	HUMAN PRESCRIPTION DRUG	potassium chloride	potassium chloride	TABLET, EXTENDED RELEASE	ORAL	20160726	N/A	ANDA	ANDA203562	Glenmark Pharmaceuticals Inc., USA	POTASSIUM CHLORIDE	1500 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-472-01)
68462-472-05	68462-472	HUMAN PRESCRIPTION DRUG	potassium chloride	potassium chloride	TABLET, EXTENDED RELEASE	ORAL	20160726	N/A	ANDA	ANDA203562	Glenmark Pharmaceuticals Inc., USA	POTASSIUM CHLORIDE	1500 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-472-05)