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
70512-841-06	70512-841	HUMAN PRESCRIPTION DRUG	Sodium Chloride	Sodium Chloride	INJECTION, SOLUTION	INTRAVENOUS	20231220	N/A	ANDA	ANDA207956	SOLA Pharmaceuticals, LLC	SODIUM CHLORIDE	9 g/1000mL	115 BAG in 1 CARTON (70512-841-06) / 50 mL in 1 BAG (70512-841-05)
70512-841-11	70512-841	HUMAN PRESCRIPTION DRUG	Sodium Chloride	Sodium Chloride	INJECTION, SOLUTION	INTRAVENOUS	20231220	N/A	ANDA	ANDA207956	SOLA Pharmaceuticals, LLC	SODIUM CHLORIDE	9 g/1000mL	70 BAG in 1 CARTON (70512-841-11) / 100 mL in 1 BAG (70512-841-10)
70512-841-26	70512-841	HUMAN PRESCRIPTION DRUG	Sodium Chloride	Sodium Chloride	INJECTION, SOLUTION	INTRAVENOUS	20231220	N/A	ANDA	ANDA207956	SOLA Pharmaceuticals, LLC	SODIUM CHLORIDE	9 g/1000mL	28 BAG in 1 CARTON (70512-841-26) / 250 mL in 1 BAG (70512-841-25)
70512-841-51	70512-841	HUMAN PRESCRIPTION DRUG	Sodium Chloride	Sodium Chloride	INJECTION, SOLUTION	INTRAVENOUS	20231220	N/A	ANDA	ANDA207956	SOLA Pharmaceuticals, LLC	SODIUM CHLORIDE	9 g/1000mL	20 BAG in 1 CARTON (70512-841-51) / 500 mL in 1 BAG (70512-841-50)
70512-841-61	70512-841	HUMAN PRESCRIPTION DRUG	Sodium Chloride	Sodium Chloride	INJECTION, SOLUTION	INTRAVENOUS	20231220	N/A	ANDA	ANDA207956	SOLA Pharmaceuticals, LLC	SODIUM CHLORIDE	9 g/1000mL	10 BAG in 1 CARTON (70512-841-61) / 1000 mL in 1 BAG (70512-841-60)