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
72888-098-00	72888-098	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	POTASSIUM CHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20230630	N/A	ANDA	ANDA216321	Advagen Pharma Ltd.	POTASSIUM CHLORIDE	1125 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-098-00)
72888-098-01	72888-098	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	POTASSIUM CHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20230630	N/A	ANDA	ANDA216321	Advagen Pharma Ltd.	POTASSIUM CHLORIDE	1125 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-098-01)
72888-097-00	72888-097	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	POTASSIUM CHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20230630	N/A	ANDA	ANDA216321	Advagen Pharma Ltd.	POTASSIUM CHLORIDE	750 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-097-00)
72888-097-01	72888-097	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	POTASSIUM CHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20230630	N/A	ANDA	ANDA216321	Advagen Pharma Ltd.	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-097-01)
72888-099-00	72888-099	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	POTASSIUM CHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20230630	N/A	ANDA	ANDA216321	Advagen Pharma Ltd.	POTASSIUM CHLORIDE	1500 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-099-00)
72888-099-01	72888-099	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	POTASSIUM CHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20230630	N/A	ANDA	ANDA216321	Advagen Pharma Ltd.	POTASSIUM CHLORIDE	1500 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-099-01)