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
65219-151-75	65219-151	HUMAN PRESCRIPTION DRUG	Potassium Chloride in Dextrose and Sodium Chloride	DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE	INJECTION, SOLUTION	INTRAVENOUS	20220902	N/A	ANDA	ANDA212348	Fresenius Kabi USA, LLC	DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE	50 g/1000mL; 1.49 g/1000mL; 2.25 g/1000mL	20 BAG in 1 CASE (65219-151-75) / 500 mL in 1 BAG (65219-151-00)
65219-153-10	65219-153	HUMAN PRESCRIPTION DRUG	Potassium Chloride in Dextrose and Sodium Chloride	DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE	INJECTION, SOLUTION	INTRAVENOUS	20220902	N/A	ANDA	ANDA212348	Fresenius Kabi USA, LLC	DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE	50 g/1000mL; 1.49 g/1000mL; 2.25 g/1000mL	10 BAG in 1 CASE (65219-153-10) / 1000 mL in 1 BAG (65219-153-02)