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
17271-701-06	17271-701	HUMAN PRESCRIPTION DRUG	Sodium chloride	SODIUM CHLORIDE	INJECTION, SOLUTION	INTRAVENOUS	20170919	N/A	ANDA	ANDA207310	Becton Dickinson and Company	SODIUM CHLORIDE	9 mg/mL	500 mL in 1 BAG (17271-701-06)
17271-701-07	17271-701	HUMAN PRESCRIPTION DRUG	Sodium chloride	SODIUM CHLORIDE	INJECTION, SOLUTION	INTRAVENOUS	20170919	N/A	ANDA	ANDA207310	Becton Dickinson and Company	SODIUM CHLORIDE	9 mg/mL	1000 mL in 1 BAG (17271-701-07)
63323-623-53	63323-623	HUMAN PRESCRIPTION DRUG	Sodium chloride	SODIUM CHLORIDE	INJECTION, SOLUTION	INTRAVENOUS	20170919	N/A	ANDA	ANDA207310	Fresenius Kabi USA, LLC	SODIUM CHLORIDE	9 mg/mL	50 mL in 1 BAG (63323-623-53)
63323-623-61	63323-623	HUMAN PRESCRIPTION DRUG	Sodium chloride	SODIUM CHLORIDE	INJECTION, SOLUTION	INTRAVENOUS	20170919	N/A	ANDA	ANDA207310	Fresenius Kabi USA, LLC	SODIUM CHLORIDE	9 mg/mL	100 mL in 1 BAG (63323-623-61)
63323-623-76	63323-623	HUMAN PRESCRIPTION DRUG	Sodium chloride	SODIUM CHLORIDE	INJECTION, SOLUTION	INTRAVENOUS	20170919	N/A	ANDA	ANDA207310	Fresenius Kabi USA, LLC	SODIUM CHLORIDE	9 mg/mL	1000 mL in 1 BAG (63323-623-76)
17271-771-02	17271-771	HUMAN PRESCRIPTION DRUG	Sodium chloride	SODIUM CHLORIDE	INJECTION, SOLUTION	INTRAVENOUS	20211117	N/A	ANDA	ANDA207310	BECTON DICKINSON AND COMPANY	SODIUM CHLORIDE	9 mg/mL	60 BAG in 1 CASE (17271-771-02) / 50 mL in 1 BAG
17271-771-03	17271-771	HUMAN PRESCRIPTION DRUG	Sodium chloride	SODIUM CHLORIDE	INJECTION, SOLUTION	INTRAVENOUS	20211117	N/A	ANDA	ANDA207310	BECTON DICKINSON AND COMPANY	SODIUM CHLORIDE	9 mg/mL	50 BAG in 1 CASE (17271-771-03) / 100 mL in 1 BAG
17271-771-05	17271-771	HUMAN PRESCRIPTION DRUG	Sodium chloride	SODIUM CHLORIDE	INJECTION, SOLUTION	INTRAVENOUS	20211117	N/A	ANDA	ANDA207310	BECTON DICKINSON AND COMPANY	SODIUM CHLORIDE	9 mg/mL	30 BAG in 1 CASE (17271-771-05) / 250 mL in 1 BAG