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
0338-0221-03	0338-0221	HUMAN PRESCRIPTION DRUG	Plasma-Lyte A	Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride and Magnesium Chloride	INJECTION, SOLUTION	INTRAVENOUS	19790202	N/A	NDA	NDA017378	Baxter Healthcare Corporation	MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE	30 mg/100mL; 37 mg/100mL; 368 mg/100mL; 526 mg/100mL; 502 mg/100mL	500 mL in 1 BAG (0338-0221-03)
0338-0221-04	0338-0221	HUMAN PRESCRIPTION DRUG	Plasma-Lyte A	Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride and Magnesium Chloride	INJECTION, SOLUTION	INTRAVENOUS	19790202	N/A	NDA	NDA017378	Baxter Healthcare Corporation	MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE	30 mg/100mL; 37 mg/100mL; 368 mg/100mL; 526 mg/100mL; 502 mg/100mL	1000 mL in 1 BAG (0338-0221-04)