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
50090-3700-1	50090-3700	HUMAN PRESCRIPTION DRUG	potassium chloride	potassium chloride	TABLET, EXTENDED RELEASE	ORAL	20160726	N/A	ANDA	ANDA203562	A-S Medication Solutions	POTASSIUM CHLORIDE	1500 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-3700-1)
50090-3700-2	50090-3700	HUMAN PRESCRIPTION DRUG	potassium chloride	potassium chloride	TABLET, EXTENDED RELEASE	ORAL	20160726	N/A	ANDA	ANDA203562	A-S Medication Solutions	POTASSIUM CHLORIDE	1500 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-3700-2)
50090-7456-0	50090-7456	HUMAN PRESCRIPTION DRUG	potassium chloride	potassium chloride	TABLET, EXTENDED RELEASE	ORAL	20241114	N/A	ANDA	ANDA203562	A-S Medication Solutions	POTASSIUM CHLORIDE	1500 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7456-0)
68462-471-01	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	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-471-01)
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)