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
24724-016-01	24724-016	HUMAN PRESCRIPTION DRUG	Metformin hydrochloride	Metformin hydrochloride	TABLET, FILM COATED	ORAL	20090603	N/A	ANDA	ANDA079148	INDICUS PHARMA LLC	METFORMIN HYDROCHLORIDE	1000 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (24724-016-01)
24724-016-50	24724-016	HUMAN PRESCRIPTION DRUG	Metformin hydrochloride	Metformin hydrochloride	TABLET, FILM COATED	ORAL	20090603	N/A	ANDA	ANDA079148	INDICUS PHARMA LLC	METFORMIN HYDROCHLORIDE	1000 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (24724-016-50)
24724-014-01	24724-014	HUMAN PRESCRIPTION DRUG	Metformin hydrochloride	Metformin hydrochloride	TABLET, FILM COATED	ORAL	20090603	N/A	ANDA	ANDA079148	INDICUS PHARMA LLC	METFORMIN HYDROCHLORIDE	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (24724-014-01)
24724-014-50	24724-014	HUMAN PRESCRIPTION DRUG	Metformin hydrochloride	Metformin hydrochloride	TABLET, FILM COATED	ORAL	20090603	N/A	ANDA	ANDA079148	INDICUS PHARMA LLC	METFORMIN HYDROCHLORIDE	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (24724-014-50)
24724-015-01	24724-015	HUMAN PRESCRIPTION DRUG	Metformin hydrochloride	Metformin hydrochloride	TABLET, FILM COATED	ORAL	20090603	N/A	ANDA	ANDA079148	INDICUS PHARMA LLC	METFORMIN HYDROCHLORIDE	850 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (24724-015-01)
24724-015-50	24724-015	HUMAN PRESCRIPTION DRUG	Metformin hydrochloride	Metformin hydrochloride	TABLET, FILM COATED	ORAL	20090603	N/A	ANDA	ANDA079148	INDICUS PHARMA LLC	METFORMIN HYDROCHLORIDE	850 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (24724-015-50)