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
63323-869-10	63323-869	HUMAN PRESCRIPTION DRUG	Dextrose and Sodium Chloride	DEXTROSE MONOHYDRATE and SODIUM CHLORIDE	INJECTION, SOLUTION	INTRAVENOUS	20201026	N/A	ANDA	ANDA211276	Fresenius Kabi USA, LLC	DEXTROSE MONOHYDRATE; SODIUM CHLORIDE	5 g/100mL; .45 g/100mL	10 BAG in 1 CASE (63323-869-10) / 1000 mL in 1 BAG (63323-869-01)
63323-869-74	63323-869	HUMAN PRESCRIPTION DRUG	Dextrose and Sodium Chloride	DEXTROSE MONOHYDRATE and SODIUM CHLORIDE	INJECTION, SOLUTION	INTRAVENOUS	20201026	N/A	ANDA	ANDA211276	Fresenius Kabi USA, LLC	DEXTROSE MONOHYDRATE; SODIUM CHLORIDE	5 g/100mL; .45 g/100mL	20 BAG in 1 CASE (63323-869-74) / 500 mL in 1 BAG (63323-869-04)
63323-869-75	63323-869	HUMAN PRESCRIPTION DRUG	Dextrose and Sodium Chloride	DEXTROSE MONOHYDRATE and SODIUM CHLORIDE	INJECTION, SOLUTION	INTRAVENOUS	20201026	N/A	ANDA	ANDA211276	Fresenius Kabi USA, LLC	DEXTROSE MONOHYDRATE; SODIUM CHLORIDE	5 g/100mL; .45 g/100mL	30 BAG in 1 CASE (63323-869-75) / 250 mL in 1 BAG (63323-869-05)