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
25021-612-81	25021-612	HUMAN PRESCRIPTION DRUG	Magnesium Sulfate	Magnesium Sulfate Heptahydrate	INJECTION, SOLUTION	INTRAVENOUS	20210215	N/A	ANDA	ANDA213917	Sagent Pharmaceuticals	MAGNESIUM SULFATE HEPTAHYDRATE	40 mg/mL	10 BAG in 1 CARTON (25021-612-81) / 50 mL in 1 BAG
25021-612-82	25021-612	HUMAN PRESCRIPTION DRUG	Magnesium Sulfate	Magnesium Sulfate Heptahydrate	INJECTION, SOLUTION	INTRAVENOUS	20210215	N/A	ANDA	ANDA213917	Sagent Pharmaceuticals	MAGNESIUM SULFATE HEPTAHYDRATE	40 mg/mL	10 BAG in 1 CARTON (25021-612-82) / 100 mL in 1 BAG
68083-397-01	68083-397	HUMAN PRESCRIPTION DRUG	MAGNESIUM SULFATE	MAGNESIUM SULFATE HEPTAHYDRATE	INJECTION, SOLUTION	INTRAVENOUS	20200710	N/A	ANDA	ANDA213917	Gland Pharma Limited	MAGNESIUM SULFATE HEPTAHYDRATE	4 g/100mL	24 POUCH in 1 CASE (68083-397-01) / 1 BAG in 1 POUCH / 100 mL in 1 BAG
68083-396-01	68083-396	HUMAN PRESCRIPTION DRUG	MAGNESIUM SULFATE	MAGNESIUM SULFATE HEPTAHYDRATE	INJECTION, SOLUTION	INTRAVENOUS	20200710	N/A	ANDA	ANDA213917	Gland Pharma Limited	MAGNESIUM SULFATE HEPTAHYDRATE	2 g/50mL	24 POUCH in 1 CASE (68083-396-01) / 1 BAG in 1 POUCH / 50 mL in 1 BAG
47335-992-01	47335-992	HUMAN PRESCRIPTION DRUG	MAGNESIUM SULFATE	magnesium sulfate heptahydrate	INJECTION, SOLUTION	INTRAVENOUS	20210801	N/A	ANDA	ANDA213917	Sun Pharmaceutical Industries, Inc.	MAGNESIUM SULFATE HEPTAHYDRATE	40 mg/mL	1 BAG in 1 POUCH (47335-992-01) / 50 mL in 1 BAG
47335-992-02	47335-992	HUMAN PRESCRIPTION DRUG	MAGNESIUM SULFATE	magnesium sulfate heptahydrate	INJECTION, SOLUTION	INTRAVENOUS	20210801	N/A	ANDA	ANDA213917	Sun Pharmaceutical Industries, Inc.	MAGNESIUM SULFATE HEPTAHYDRATE	40 mg/mL	1 BAG in 1 POUCH (47335-992-02) / 100 mL in 1 BAG