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
68071-3518-9	68071-3518	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	metformin hydrochloride	TABLET	ORAL	20231006	N/A	ANDA	ANDA213320	NuCare Pharmaceuticals,Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	90 TABLET in 1 BOTTLE (68071-3518-9)
68071-3526-1	68071-3526	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	metformin hydrochloride	TABLET	ORAL	20231023	N/A	ANDA	ANDA213320	NuCare Pharmaceuticals,Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	100 TABLET in 1 BOTTLE (68071-3526-1)
68071-3531-1	68071-3531	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	metformin hydrochloride	TABLET	ORAL	20231128	N/A	ANDA	ANDA213320	NuCare Pharmaceuticals,Inc.	METFORMIN HYDROCHLORIDE	850 mg/1	100 TABLET in 1 BOTTLE (68071-3531-1)
68071-3575-8	68071-3575	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	metformin hydrochloride	TABLET	ORAL	20240216	N/A	ANDA	ANDA213320	NuCare Pharmaceuticals,Inc.	METFORMIN HYDROCHLORIDE	850 mg/1	180 TABLET in 1 BOTTLE (68071-3575-8)
71335-2466-7	71335-2466	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	metformin hydrochloride	TABLET	ORAL	20240816	N/A	ANDA	ANDA213320	Bryant Ranch Prepack	METFORMIN HYDROCHLORIDE	500 mg/1	56 TABLET in 1 BOTTLE (71335-2466-7)
71335-2466-8	71335-2466	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	metformin hydrochloride	TABLET	ORAL	20240816	N/A	ANDA	ANDA213320	Bryant Ranch Prepack	METFORMIN HYDROCHLORIDE	500 mg/1	180 TABLET in 1 BOTTLE (71335-2466-8)
71335-2466-9	71335-2466	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	metformin hydrochloride	TABLET	ORAL	20240816	N/A	ANDA	ANDA213320	Bryant Ranch Prepack	METFORMIN HYDROCHLORIDE	500 mg/1	10 TABLET in 1 BOTTLE (71335-2466-9)