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
0338-0673-04	0338-0673	HUMAN PRESCRIPTION DRUG	Potassium Chloride in Dextrose and Sodium Chloride	Potassium Chloride, Dextrose Monohydrate and Sodium Chloride	INJECTION, SOLUTION	INTRAVENOUS	19790202	N/A	NDA	NDA018008	Baxter Healthcare Corporation	DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE	5 g/100mL; 224 mg/100mL; 450 mg/100mL	1000 mL in 1 BAG (0338-0673-04)
0338-0675-04	0338-0675	HUMAN PRESCRIPTION DRUG	Potassium Chloride in Dextrose and Sodium Chloride	Potassium Chloride, Dextrose Monohydrate and Sodium Chloride	INJECTION, SOLUTION	INTRAVENOUS	19790202	N/A	NDA	NDA018008	Baxter Healthcare Corporation	DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE	5 g/100mL; 300 mg/100mL; 450 mg/100mL	1000 mL in 1 BAG (0338-0675-04)
0338-0669-04	0338-0669	HUMAN PRESCRIPTION DRUG	Potassium Chloride in Dextrose and Sodium Chloride	Potassium Chloride, Dextrose Monohydrate and Sodium Chloride	INJECTION, SOLUTION	INTRAVENOUS	19790202	N/A	NDA	NDA018008	Baxter Healthcare Corporation	DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE	5 g/100mL; 75 mg/100mL; 450 mg/100mL	1000 mL in 1 BAG (0338-0669-04)
0338-0671-03	0338-0671	HUMAN PRESCRIPTION DRUG	Potassium Chloride in Dextrose and Sodium Chloride	Potassium Chloride, Dextrose Monohydrate and Sodium Chloride	INJECTION, SOLUTION	INTRAVENOUS	19790202	N/A	NDA	NDA018008	Baxter Healthcare Corporation	DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE	5 g/100mL; 150 mg/100mL; 450 mg/100mL	500 mL in 1 BAG (0338-0671-03)
0338-0671-04	0338-0671	HUMAN PRESCRIPTION DRUG	Potassium Chloride in Dextrose and Sodium Chloride	Potassium Chloride, Dextrose Monohydrate and Sodium Chloride	INJECTION, SOLUTION	INTRAVENOUS	19790202	N/A	NDA	NDA018008	Baxter Healthcare Corporation	DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE	5 g/100mL; 150 mg/100mL; 450 mg/100mL	1000 mL in 1 BAG (0338-0671-04)