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
65841-715-01	65841-715	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20090923	N/A	ANDA	ANDA090411	Zydus Lifesciences Limited	ROPINIROLE HYDROCHLORIDE	2 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-715-01)
65841-715-10	65841-715	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20090923	N/A	ANDA	ANDA090411	Zydus Lifesciences Limited	ROPINIROLE HYDROCHLORIDE	2 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65841-715-10)
65841-712-01	65841-712	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20090923	N/A	ANDA	ANDA090411	Zydus Lifesciences Limited	ROPINIROLE HYDROCHLORIDE	.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-712-01)
65841-712-10	65841-712	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20090923	N/A	ANDA	ANDA090411	Zydus Lifesciences Limited	ROPINIROLE HYDROCHLORIDE	.25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65841-712-10)
65841-716-01	65841-716	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20090923	N/A	ANDA	ANDA090411	Zydus Lifesciences Limited	ROPINIROLE HYDROCHLORIDE	3 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-716-01)
65841-716-10	65841-716	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20090923	N/A	ANDA	ANDA090411	Zydus Lifesciences Limited	ROPINIROLE HYDROCHLORIDE	3 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65841-716-10)
65841-714-01	65841-714	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20090923	N/A	ANDA	ANDA090411	Zydus Lifesciences Limited	ROPINIROLE HYDROCHLORIDE	1 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-714-01)
65841-714-10	65841-714	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20090923	N/A	ANDA	ANDA090411	Zydus Lifesciences Limited	ROPINIROLE HYDROCHLORIDE	1 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65841-714-10)
65841-718-01	65841-718	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20090923	N/A	ANDA	ANDA090411	Zydus Lifesciences Limited	ROPINIROLE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-718-01)
65841-718-10	65841-718	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20090923	N/A	ANDA	ANDA090411	Zydus Lifesciences Limited	ROPINIROLE HYDROCHLORIDE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65841-718-10)
65841-713-01	65841-713	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20090923	N/A	ANDA	ANDA090411	Zydus Lifesciences Limited	ROPINIROLE HYDROCHLORIDE	.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-713-01)
65841-713-10	65841-713	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20090923	N/A	ANDA	ANDA090411	Zydus Lifesciences Limited	ROPINIROLE HYDROCHLORIDE	.5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65841-713-10)
65841-717-01	65841-717	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20090923	N/A	ANDA	ANDA090411	Zydus Lifesciences Limited	ROPINIROLE HYDROCHLORIDE	4 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-717-01)
65841-717-10	65841-717	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20090923	N/A	ANDA	ANDA090411	Zydus Lifesciences Limited	ROPINIROLE HYDROCHLORIDE	4 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65841-717-10)