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
65219-119-10	65219-119	HUMAN PRESCRIPTION DRUG	Potassium Chloride in Dextrose and Sodium Chloride	DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE	INJECTION, SOLUTION	INTRAVENOUS	20220831	N/A	ANDA	ANDA213445	Fresenius Kabi USA, LLC	DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE	50 g/1000mL; 2.98 g/1000mL; 9 g/1000mL	10 BAG in 1 CASE (65219-119-10) / 1000 mL in 1 BAG (65219-119-01)
65219-118-10	65219-118	HUMAN PRESCRIPTION DRUG	Potassium Chloride in Dextrose and Sodium Chloride	DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE	INJECTION, SOLUTION	INTRAVENOUS	20220831	N/A	ANDA	ANDA213445	Fresenius Kabi USA, LLC	DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE	50 g/1000mL; 1.49 g/1000mL; 9 g/1000mL	10 BAG in 1 CASE (65219-118-10) / 1000 mL in 1 BAG (65219-118-01)