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
68788-8756-6	68788-8756	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20241014	N/A	ANDA	ANDA209882	Preferred Pharmaceuticals Inc.	METFORMIN HYDROCHLORIDE	850 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-8756-6)
68788-8756-8	68788-8756	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20241014	N/A	ANDA	ANDA209882	Preferred Pharmaceuticals Inc.	METFORMIN HYDROCHLORIDE	850 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (68788-8756-8)
68788-8756-9	68788-8756	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20241014	N/A	ANDA	ANDA209882	Preferred Pharmaceuticals Inc.	METFORMIN HYDROCHLORIDE	850 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-8756-9)
68071-3833-8	68071-3833	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20250418	N/A	ANDA	ANDA209882	NuCare Pharmaceuticals,Inc.	METFORMIN HYDROCHLORIDE	850 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (68071-3833-8)