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
70710-1391-9	70710-1391	HUMAN PRESCRIPTION DRUG	Droxidopa	Droxidopa	CAPSULE	ORAL	20210219	N/A	ANDA	ANDA211818	Zydus Pharmaceuticals USA Inc.	DROXIDOPA	300 mg/1	90 CAPSULE in 1 BOTTLE (70710-1391-9)
70710-1390-9	70710-1390	HUMAN PRESCRIPTION DRUG	Droxidopa	Droxidopa	CAPSULE	ORAL	20210219	N/A	ANDA	ANDA211818	Zydus Pharmaceuticals USA Inc.	DROXIDOPA	200 mg/1	90 CAPSULE in 1 BOTTLE (70710-1390-9)
70710-1389-9	70710-1389	HUMAN PRESCRIPTION DRUG	Droxidopa	Droxidopa	CAPSULE	ORAL	20210219	N/A	ANDA	ANDA211818	Zydus Pharmaceuticals USA Inc.	DROXIDOPA	100 mg/1	90 CAPSULE in 1 BOTTLE (70710-1389-9)
70771-1609-9	70771-1609	HUMAN PRESCRIPTION DRUG	Droxidopa	Droxidopa	CAPSULE	ORAL	20210219	N/A	ANDA	ANDA211818	Zydus Lifesciences Limited	DROXIDOPA	100 mg/1	90 CAPSULE in 1 BOTTLE (70771-1609-9)
70771-1610-9	70771-1610	HUMAN PRESCRIPTION DRUG	Droxidopa	Droxidopa	CAPSULE	ORAL	20210219	N/A	ANDA	ANDA211818	Zydus Lifesciences Limited	DROXIDOPA	200 mg/1	90 CAPSULE in 1 BOTTLE (70771-1610-9)
70771-1611-9	70771-1611	HUMAN PRESCRIPTION DRUG	Droxidopa	Droxidopa	CAPSULE	ORAL	20210219	N/A	ANDA	ANDA211818	Zydus Lifesciences Limited	DROXIDOPA	300 mg/1	90 CAPSULE in 1 BOTTLE (70771-1611-9)