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
50090-6856-4	50090-6856	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20231201	N/A	ANDA	ANDA209882	A-S Medication Solutions	METFORMIN HYDROCHLORIDE	1000 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-6856-4)
50090-6856-5	50090-6856	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20231201	N/A	ANDA	ANDA209882	A-S Medication Solutions	METFORMIN HYDROCHLORIDE	1000 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (50090-6856-5)
42385-949-18	42385-949	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20210720	N/A	ANDA	ANDA209882	Laurus Labs Limited	METFORMIN HYDROCHLORIDE	1000 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (42385-949-18)
42385-949-19	42385-949	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20210517	N/A	ANDA	ANDA209882	Laurus Labs Limited	METFORMIN HYDROCHLORIDE	1000 mg/1	10 BLISTER PACK in 1 CARTON (42385-949-19) / 10 TABLET, FILM COATED in 1 BLISTER PACK
42385-949-60	42385-949	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20210517	N/A	ANDA	ANDA209882	Laurus Labs Limited	METFORMIN HYDROCHLORIDE	1000 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (42385-949-60)
42385-949-90	42385-949	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20220801	N/A	ANDA	ANDA209882	Laurus Labs Limited	METFORMIN HYDROCHLORIDE	1000 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (42385-949-90)