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
43386-917-05	43386-917	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20170130	N/A	ANDA	ANDA206347	Lupin Pharmaceuticals,Inc.	POTASSIUM CHLORIDE	20 meq/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-917-05)
43386-917-10	43386-917	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20170130	N/A	ANDA	ANDA206347	Lupin Pharmaceuticals,Inc.	POTASSIUM CHLORIDE	20 meq/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-917-10)
43386-915-01	43386-915	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20160121	N/A	ANDA	ANDA206347	Lupin Pharmaceuticals,Inc.	POTASSIUM CHLORIDE	10 meq/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-915-01)
43386-915-10	43386-915	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20170130	N/A	ANDA	ANDA206347	Lupin Pharmaceuticals,Inc.	POTASSIUM CHLORIDE	10 meq/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-915-10)
43386-917-01	43386-917	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20160121	N/A	ANDA	ANDA206347	Lupin Pharmaceuticals,Inc.	POTASSIUM CHLORIDE	20 meq/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-917-01)