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
63323-090-20	63323-090	HUMAN PRESCRIPTION DRUG	Sodium Chloride	Sodium Chloride	INJECTION, SOLUTION, CONCENTRATE	INTRAVENOUS	20210428	N/A	ANDA	ANDA212070	Fresenius Kabi USA, LLC	SODIUM CHLORIDE	2.5 meq/mL	25 VIAL, PLASTIC in 1 TRAY (63323-090-20) / 20 mL in 1 VIAL, PLASTIC (63323-090-02)
63323-090-40	63323-090	HUMAN PRESCRIPTION DRUG	Sodium Chloride	Sodium Chloride	INJECTION, SOLUTION, CONCENTRATE	INTRAVENOUS	20210428	N/A	ANDA	ANDA212070	Fresenius Kabi USA, LLC	SODIUM CHLORIDE	2.5 meq/mL	25 VIAL, PLASTIC in 1 TRAY (63323-090-40) / 40 mL in 1 VIAL, PLASTIC (63323-090-04)
63323-095-61	63323-095	HUMAN PRESCRIPTION DRUG	Sodium Chloride	Sodium Chloride	INJECTION, SOLUTION, CONCENTRATE	INTRAVENOUS	20220214	N/A	ANDA	ANDA212070	Fresenius Kabi USA, LLC	SODIUM CHLORIDE	4 meq/mL	20 VIAL, PLASTIC in 1 TRAY (63323-095-61) / 100 mL in 1 VIAL, PLASTIC (63323-095-02)