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
52817-324-10	52817-324	HUMAN PRESCRIPTION DRUG	Midodrine Hydrochloride	Midodrine Hydrochloride	TABLET	ORAL	20190819	N/A	ANDA	ANDA212543	TruPharma, LLC	MIDODRINE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (52817-324-10)
72888-114-01	72888-114	HUMAN PRESCRIPTION DRUG	Midodrine Hydrochloride	Midodrine Hydrochloride	TABLET	ORAL	20190819	N/A	ANDA	ANDA212543	Advagen Pharma Limited	MIDODRINE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (72888-114-01)
52817-323-10	52817-323	HUMAN PRESCRIPTION DRUG	Midodrine Hydrochloride	Midodrine Hydrochloride	TABLET	ORAL	20190819	N/A	ANDA	ANDA212543	TruPharma, LLC	MIDODRINE HYDROCHLORIDE	2.5 mg/1	100 TABLET in 1 BOTTLE (52817-323-10)
72888-112-01	72888-112	HUMAN PRESCRIPTION DRUG	Midodrine Hydrochloride	Midodrine Hydrochloride	TABLET	ORAL	20190819	N/A	ANDA	ANDA212543	Advagen Pharma Limited	MIDODRINE HYDROCHLORIDE	2.5 mg/1	100 TABLET in 1 BOTTLE (72888-112-01)
52817-325-10	52817-325	HUMAN PRESCRIPTION DRUG	Midodrine Hydrochloride	Midodrine Hydrochloride	TABLET	ORAL	20190819	N/A	ANDA	ANDA212543	TruPharma, LLC	MIDODRINE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (52817-325-10)
71335-2171-1	71335-2171	HUMAN PRESCRIPTION DRUG	Midodrine Hydrochloride	Midodrine Hydrochloride	TABLET	ORAL	20230414	N/A	ANDA	ANDA212543	Bryant Ranch Prepack	MIDODRINE HYDROCHLORIDE	5 mg/1	30 TABLET in 1 BOTTLE (71335-2171-1)
72888-113-01	72888-113	HUMAN PRESCRIPTION DRUG	Midodrine Hydrochloride	Midodrine Hydrochloride	TABLET	ORAL	20190819	N/A	ANDA	ANDA212543	Advagen Pharma Limited	MIDODRINE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (72888-113-01)