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
59651-549-01	59651-549	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240415	N/A	ANDA	ANDA079118	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	750 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-549-01)
59651-549-05	59651-549	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240415	N/A	ANDA	ANDA079118	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	750 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-549-05)
59651-548-99	59651-548	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240415	N/A	ANDA	ANDA079118	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	500 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-548-99)
59651-548-05	59651-548	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240415	N/A	ANDA	ANDA079118	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	500 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-548-05)
59651-548-01	59651-548	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240415	N/A	ANDA	ANDA079118	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	500 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-548-01)