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
70518-3130-1	70518-3130	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20250422	N/A	ANDA	ANDA077095	REMEDYREPACK INC.	METFORMIN HYDROCHLORIDE	1000 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3130-1)
70518-3130-2	70518-3130	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20250714	N/A	ANDA	ANDA077095	REMEDYREPACK INC.	METFORMIN HYDROCHLORIDE	1000 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3130-2)
51655-649-25	51655-649	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20250723	N/A	ANDA	ANDA077095	Northwind Health Company, LLC	METFORMIN HYDROCHLORIDE	1000 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-25)
51655-649-26	51655-649	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20230623	N/A	ANDA	ANDA077095	Northwind Health Company, LLC	METFORMIN HYDROCHLORIDE	1000 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-26)
51655-649-52	51655-649	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20210401	N/A	ANDA	ANDA077095	Northwind Health Company, LLC	METFORMIN HYDROCHLORIDE	1000 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-52)
0615-8578-05	0615-8578	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20250417	N/A	ANDA	ANDA077095	NCS HealthCare of KY, LLC dba Vangard Labs	METFORMIN HYDROCHLORIDE	1000 mg/1	15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8578-05)
0615-8578-39	0615-8578	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20250417	N/A	ANDA	ANDA077095	NCS HealthCare of KY, LLC dba Vangard Labs	METFORMIN HYDROCHLORIDE	1000 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8578-39)
71610-920-53	71610-920	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20250701	N/A	ANDA	ANDA077095	Aphena Pharma Solutions - Tennessee, LLC	METFORMIN HYDROCHLORIDE	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71610-920-53)
71610-920-60	71610-920	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20250701	N/A	ANDA	ANDA077095	Aphena Pharma Solutions - Tennessee, LLC	METFORMIN HYDROCHLORIDE	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71610-920-60)
71610-920-80	71610-920	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20250701	N/A	ANDA	ANDA077095	Aphena Pharma Solutions - Tennessee, LLC	METFORMIN HYDROCHLORIDE	500 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71610-920-80)
0615-8629-05	0615-8629	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20260331	N/A	ANDA	ANDA077095	NCS HealthCare of KY, LLC dba Vangard Labs	METFORMIN HYDROCHLORIDE	500 mg/1	15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8629-05)
0615-8629-28	0615-8629	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20260331	N/A	ANDA	ANDA077095	NCS HealthCare of KY, LLC dba Vangard Labs	METFORMIN HYDROCHLORIDE	500 mg/1	28 TABLET, FILM COATED in 1 BLISTER PACK (0615-8629-28)
0615-8629-30	0615-8629	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20260414	N/A	ANDA	ANDA077095	NCS HealthCare of KY, LLC dba Vangard Labs	METFORMIN HYDROCHLORIDE	500 mg/1	6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8629-30) / 5 TABLET, FILM COATED in 1 BLISTER PACK
0615-8629-39	0615-8629	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20260331	N/A	ANDA	ANDA077095	NCS HealthCare of KY, LLC dba Vangard Labs	METFORMIN HYDROCHLORIDE	500 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8629-39)
65862-010-01	65862-010	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20050114	N/A	ANDA	ANDA077095	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	1000 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-010-01)
65862-010-05	65862-010	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20050114	N/A	ANDA	ANDA077095	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	1000 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-010-05)
65862-010-33	65862-010	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20050114	N/A	ANDA	ANDA077095	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	1000 mg/1	300 TABLET, FILM COATED in 1 BOTTLE (65862-010-33)
65862-010-46	65862-010	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20050114	N/A	ANDA	ANDA077095	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	1000 mg/1	2000 TABLET, FILM COATED in 1 BOTTLE (65862-010-46)
65862-010-50	65862-010	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20050114	N/A	ANDA	ANDA077095	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	1000 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (65862-010-50)
65862-010-60	65862-010	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20050114	N/A	ANDA	ANDA077095	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	1000 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (65862-010-60)