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
51662-1521-1	51662-1521	HUMAN PRESCRIPTION DRUG	LACTATED RINGERS AND DEXTROSE	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, AND DEXTROSE MONOHYDRATE	INJECTION, SOLUTION	INTRAVENOUS	20200521	N/A	NDA	NDA017608	HF Acquisition Co LLC, DBA HealthFirst	CALCIUM CHLORIDE; DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE	20 mg/100mL; 5 g/100mL; 30 mg/100mL; 600 mg/100mL; 310 mg/100mL	1000 mL in 1 BAG (51662-1521-1)
51662-1229-1	51662-1229	HUMAN PRESCRIPTION DRUG	LACTATED RINGERS AND DEXTROSE	SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM CHLORIDE, DEXTROSE	INJECTION, SOLUTION	INTRAVENOUS	20181006	N/A	NDA	NDA017608	HF Acquisition Co LLC, DBA HealthFirst	CALCIUM CHLORIDE; DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE	20 mg/100mL; 5 g/100mL; 30 mg/100mL; 600 mg/100mL; 310 mg/100mL	1 BAG in 1 POUCH (51662-1229-1) / 1000 mL in 1 BAG
0990-7929-09	0990-7929	HUMAN PRESCRIPTION DRUG	Lactated Ringers and Dextrose	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, and DEXTROSE MONOHYDRATE	INJECTION, SOLUTION	INTRAVENOUS	20190801	N/A	NDA	NDA017608	ICU Medical Inc.	CALCIUM CHLORIDE; DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE	20 mg/100mL; 5 g/100mL; 30 mg/100mL; 600 mg/100mL; 310 mg/100mL	12 POUCH in 1 CASE (0990-7929-09) / 1 BAG in 1 POUCH / 1000 mL in 1 BAG
0990-7929-03	0990-7929	HUMAN PRESCRIPTION DRUG	Lactated Ringers and Dextrose	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, and DEXTROSE MONOHYDRATE	INJECTION, SOLUTION	INTRAVENOUS	20190801	N/A	NDA	NDA017608	ICU Medical Inc.	CALCIUM CHLORIDE; DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE	20 mg/100mL; 5 g/100mL; 30 mg/100mL; 600 mg/100mL; 310 mg/100mL	24 POUCH in 1 CASE (0990-7929-03) / 1 BAG in 1 POUCH / 500 mL in 1 BAG