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
68462-521-01	68462-521	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20191125	N/A	ANDA	ANDA212969	GLENMARK PHARMACEUTICALS INC., USA	METFORMIN HYDROCHLORIDE	1000 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-521-01)
68462-521-05	68462-521	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20191125	N/A	ANDA	ANDA212969	GLENMARK PHARMACEUTICALS INC., USA	METFORMIN HYDROCHLORIDE	1000 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-521-05)
68462-521-90	68462-521	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20191125	N/A	ANDA	ANDA212969	GLENMARK PHARMACEUTICALS INC., USA	METFORMIN HYDROCHLORIDE	1000 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-521-90)
68462-520-10	68462-520	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20191125	N/A	ANDA	ANDA212969	GLENMARK PHARMACEUTICALS INC., USA	METFORMIN HYDROCHLORIDE	500 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-520-10)
68462-520-05	68462-520	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20191125	N/A	ANDA	ANDA212969	GLENMARK PHARMACEUTICALS INC., USA	METFORMIN HYDROCHLORIDE	500 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-520-05)
68462-520-01	68462-520	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20191125	N/A	ANDA	ANDA212969	GLENMARK PHARMACEUTICALS INC., USA	METFORMIN HYDROCHLORIDE	500 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-520-01)