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
40032-912-05	40032-912	HUMAN PRESCRIPTION DRUG	potassium chloride	potassium chloride	TABLET, EXTENDED RELEASE	ORAL	20160809	N/A	ANDA	ANDA206759	Novel Laboratories, Inc.	POTASSIUM CHLORIDE	8 meq/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (40032-912-05)
40032-912-11	40032-912	HUMAN PRESCRIPTION DRUG	potassium chloride	potassium chloride	TABLET, EXTENDED RELEASE	ORAL	20160809	N/A	ANDA	ANDA206759	Novel Laboratories, Inc.	POTASSIUM CHLORIDE	8 meq/1	750 TABLET, EXTENDED RELEASE in 1 BOTTLE (40032-912-11)
40032-912-01	40032-912	HUMAN PRESCRIPTION DRUG	potassium chloride	potassium chloride	TABLET, EXTENDED RELEASE	ORAL	20160809	N/A	ANDA	ANDA206759	Novel Laboratories, Inc.	POTASSIUM CHLORIDE	8 meq/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (40032-912-01)
40032-913-01	40032-913	HUMAN PRESCRIPTION DRUG	potassium chloride	potassium chloride	TABLET, EXTENDED RELEASE	ORAL	20160809	N/A	ANDA	ANDA206759	Novel Laboratories, Inc.	POTASSIUM CHLORIDE	10 meq/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (40032-913-01)
40032-913-05	40032-913	HUMAN PRESCRIPTION DRUG	potassium chloride	potassium chloride	TABLET, EXTENDED RELEASE	ORAL	20160809	N/A	ANDA	ANDA206759	Novel Laboratories, Inc.	POTASSIUM CHLORIDE	10 meq/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (40032-913-05)