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
68382-759-01	68382-759	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Pharmaceuticals USA Inc.	METFORMIN HYDROCHLORIDE	850 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-759-01)
68382-759-05	68382-759	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Pharmaceuticals USA Inc.	METFORMIN HYDROCHLORIDE	850 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68382-759-05)
68382-759-10	68382-759	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Pharmaceuticals USA Inc.	METFORMIN HYDROCHLORIDE	850 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-759-10)
68382-759-16	68382-759	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Pharmaceuticals USA Inc.	METFORMIN HYDROCHLORIDE	850 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68382-759-16)
68382-759-77	68382-759	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Pharmaceuticals USA Inc.	METFORMIN HYDROCHLORIDE	850 mg/1	100 BLISTER PACK in 1 CARTON (68382-759-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68382-759-30)
68382-760-01	68382-760	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Pharmaceuticals USA Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-760-01)
68382-760-05	68382-760	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Pharmaceuticals USA Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68382-760-05)
68382-760-10	68382-760	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Pharmaceuticals USA Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-760-10)
68382-760-16	68382-760	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Pharmaceuticals USA Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68382-760-16)
68382-760-77	68382-760	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Pharmaceuticals USA Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	100 BLISTER PACK in 1 CARTON (68382-760-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68382-760-30)
68382-758-05	68382-758	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Pharmaceuticals USA Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68382-758-05)
68382-758-10	68382-758	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Pharmaceuticals USA Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-758-10)
68382-758-16	68382-758	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Pharmaceuticals USA Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68382-758-16)