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
71335-0776-4	71335-0776	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180417	N/A	ANDA	ANDA078321	Bryant Ranch Prepack	METFORMIN HYDROCHLORIDE	750 mg/1	180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-4)
71205-186-20	71205-186	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20181201	N/A	ANDA	ANDA078321	Proficient Rx LP	METFORMIN HYDROCHLORIDE	500 mg/1	20 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-186-20)
71205-186-90	71205-186	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20181201	N/A	ANDA	ANDA078321	Proficient Rx LP	METFORMIN HYDROCHLORIDE	500 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-186-90)
71205-186-30	71205-186	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20181201	N/A	ANDA	ANDA078321	Proficient Rx LP	METFORMIN HYDROCHLORIDE	500 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-186-30)
71205-186-60	71205-186	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20181201	N/A	ANDA	ANDA078321	Proficient Rx LP	METFORMIN HYDROCHLORIDE	500 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-186-60)
71205-186-72	71205-186	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20181201	N/A	ANDA	ANDA078321	Proficient Rx LP	METFORMIN HYDROCHLORIDE	500 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-186-72)