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
71610-447-60	71610-447	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200724	N/A	ANDA	ANDA077336	Aphena Pharma Solutions - Tennessee, LLC	METFORMIN HYDROCHLORIDE	500 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-447-60)
71610-447-70	71610-447	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200724	N/A	ANDA	ANDA077336	Aphena Pharma Solutions - Tennessee, LLC	METFORMIN HYDROCHLORIDE	500 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-447-70)
71610-447-80	71610-447	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200724	N/A	ANDA	ANDA077336	Aphena Pharma Solutions - Tennessee, LLC	METFORMIN HYDROCHLORIDE	500 mg/1	180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-447-80)
71610-447-94	71610-447	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20210311	N/A	ANDA	ANDA077336	Aphena Pharma Solutions - Tennessee, LLC	METFORMIN HYDROCHLORIDE	500 mg/1	360 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-447-94)
68788-8532-1	68788-8532	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20231003	N/A	ANDA	ANDA077336	Preferred Pharmaceuticals Inc.	METFORMIN HYDROCHLORIDE	750 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8532-1)
71610-447-53	71610-447	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200724	N/A	ANDA	ANDA077336	Aphena Pharma Solutions - Tennessee, LLC	METFORMIN HYDROCHLORIDE	500 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-447-53)
71610-447-30	71610-447	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200724	N/A	ANDA	ANDA077336	Aphena Pharma Solutions - Tennessee, LLC	METFORMIN HYDROCHLORIDE	500 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-447-30)
71610-441-53	71610-441	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200624	N/A	ANDA	ANDA077336	Aphena Pharma Solutions - Tennessee, LLC	METFORMIN HYDROCHLORIDE	750 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-441-53)
62756-142-01	62756-142	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20060209	N/A	ANDA	ANDA077336	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-142-01)
62756-142-02	62756-142	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20060209	N/A	ANDA	ANDA077336	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-142-02)
62756-143-01	62756-143	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20060209	N/A	ANDA	ANDA077336	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	750 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-143-01)