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
50090-7106-2	50090-7106	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240306	N/A	ANDA	ANDA209882	A-S Medication Solutions	METFORMIN HYDROCHLORIDE	850 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (50090-7106-2)
50090-7107-0	50090-7107	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240306	N/A	ANDA	ANDA209882	A-S Medication Solutions	METFORMIN HYDROCHLORIDE	850 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-7107-0)
50090-7106-4	50090-7106	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240306	N/A	ANDA	ANDA209882	A-S Medication Solutions	METFORMIN HYDROCHLORIDE	850 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-7106-4)
50090-7106-5	50090-7106	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240306	N/A	ANDA	ANDA209882	A-S Medication Solutions	METFORMIN HYDROCHLORIDE	850 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (50090-7106-5)
50090-7106-0	50090-7106	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240306	N/A	ANDA	ANDA209882	A-S Medication Solutions	METFORMIN HYDROCHLORIDE	850 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-7106-0)
50090-7866-0	50090-7866	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20260126	N/A	ANDA	ANDA209882	A-S Medication Solutions	METFORMIN HYDROCHLORIDE	1000 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-7866-0)