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
60687-143-01	60687-143	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20150909	N/A	ANDA	ANDA203686	American Health Packaging	METFORMIN HYDROCHLORIDE	850 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-143-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-143-11)
82009-174-10	82009-174	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20250718	N/A	ANDA	ANDA203686	Quallent Pharmaceuticals Health LLC	METFORMIN HYDROCHLORIDE	500 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (82009-174-10)
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)
65841-809-01	65841-809	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-809-01)
65841-809-05	65841-809	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65841-809-05)
65841-809-10	65841-809	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE	500 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65841-809-10)
65841-809-16	65841-809	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65841-809-16)
65841-809-77	65841-809	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE	500 mg/1	100 BLISTER PACK in 1 CARTON (65841-809-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (65841-809-30)
60687-155-01	60687-155	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20160404	N/A	ANDA	ANDA203686	American Health Packaging	METFORMIN HYDROCHLORIDE	500 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-155-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-155-11)
82009-175-10	82009-175	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20250718	N/A	ANDA	ANDA203686	Quallent Pharmaceuticals Health LLC	METFORMIN HYDROCHLORIDE	1000 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (82009-175-10)
65841-811-01	65841-811	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE	1000 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-811-01)
65841-811-05	65841-811	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE	1000 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65841-811-05)
65841-811-10	65841-811	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE	1000 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65841-811-10)
65841-811-16	65841-811	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE	1000 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65841-811-16)
65841-811-77	65841-811	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141209	N/A	ANDA	ANDA203686	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE	1000 mg/1	100 BLISTER PACK in 1 CARTON (65841-811-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (65841-811-30)
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)