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
70756-050-11	70756-050	HUMAN PRESCRIPTION DRUG	Midodrine Hydrochloride	Midodrine Hydrochloride	TABLET	ORAL	20231101	N/A	ANDA	ANDA217271	Lifestar Pharma LLC	MIDODRINE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (70756-050-11)
70756-049-11	70756-049	HUMAN PRESCRIPTION DRUG	Midodrine Hydrochloride	Midodrine Hydrochloride	TABLET	ORAL	20231101	N/A	ANDA	ANDA217271	Lifestar Pharma LLC	MIDODRINE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (70756-049-11)
81469-141-90	81469-141	HUMAN PRESCRIPTION DRUG	Midodrine Hydrochloride	Midodrine Hydrochloride	TABLET	ORAL	20250813	N/A	ANDA	ANDA217271	First Nation Group, LLC	MIDODRINE HYDROCHLORIDE	10 mg/1	90 TABLET in 1 BOTTLE (81469-141-90)
70756-010-11	70756-010	HUMAN PRESCRIPTION DRUG	Midodrine Hydrochloride	Midodrine Hydrochloride	TABLET	ORAL	20231101	N/A	ANDA	ANDA217271	Lifestar Pharma LLC	MIDODRINE HYDROCHLORIDE	2.5 mg/1	100 TABLET in 1 BOTTLE (70756-010-11)
81469-140-90	81469-140	HUMAN PRESCRIPTION DRUG	Midodrine Hydrochloride	Midodrine Hydrochloride	TABLET	ORAL	20250813	N/A	ANDA	ANDA217271	First Nation Group, LLC	MIDODRINE HYDROCHLORIDE	5 mg/1	90 TABLET in 1 BOTTLE (81469-140-90)
81469-139-90	81469-139	HUMAN PRESCRIPTION DRUG	Midodrine Hydrochloride	Midodrine Hydrochloride	TABLET	ORAL	20250813	N/A	ANDA	ANDA217271	First Nation Group, LLC	MIDODRINE HYDROCHLORIDE	2.5 mg/1	90 TABLET in 1 BOTTLE (81469-139-90)
67046-1512-3	67046-1512	HUMAN PRESCRIPTION DRUG	Midodrine Hydrochloride	Midodrine Hydrochloride	TABLET	ORAL	20250201	N/A	ANDA	ANDA217271	Coupler LLC	MIDODRINE HYDROCHLORIDE	5 mg/1	30 TABLET in 1 BLISTER PACK (67046-1512-3)