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
68788-8520-6	68788-8520	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230901	N/A	ANDA	ANDA090692	Preferred Pharmaceuticals, Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8520-6)
70518-4369-0	70518-4369	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250624	N/A	ANDA	ANDA090692	REMEDYREPACK INC.	METFORMIN HYDROCHLORIDE	1000 mg/1	30 POUCH in 1 BOX (70518-4369-0) / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-4369-1)
63629-5934-1	63629-5934	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250602	N/A	ANDA	ANDA090692	Bryant Ranch Prepack	METFORMIN HYDROCHLORIDE	1000 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-5934-1)
63629-5934-3	63629-5934	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250602	N/A	ANDA	ANDA090692	Bryant Ranch Prepack	METFORMIN HYDROCHLORIDE	1000 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-5934-3)
68180-336-07	68180-336	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20110930	N/A	ANDA	ANDA090692	Lupin Pharmaceuticals, Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-336-07)
68180-337-07	68180-337	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20110930	N/A	ANDA	ANDA090692	Lupin Pharmaceuticals, Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-337-07)
63629-5934-2	63629-5934	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250602	N/A	ANDA	ANDA090692	Bryant Ranch Prepack	METFORMIN HYDROCHLORIDE	1000 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-5934-2)