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
0228-3658-03	0228-3658	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120823	N/A	ANDA	ANDA090869	Actavis Pharma, Inc.	ROPINIROLE HYDROCHLORIDE	2 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-3658-03)
0228-3658-09	0228-3658	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120823	N/A	ANDA	ANDA090869	Actavis Pharma, Inc.	ROPINIROLE HYDROCHLORIDE	2 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-3658-09)
42291-715-30	42291-715	HUMAN PRESCRIPTION DRUG	Ropinirole Hydrochloride	Ropinirole Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231101	N/A	ANDA	ANDA090869	AvKARE	ROPINIROLE HYDROCHLORIDE	6 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-715-30)
0228-3659-03	0228-3659	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120823	N/A	ANDA	ANDA090869	Actavis Pharma, Inc.	ROPINIROLE HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-3659-03)
0228-3659-09	0228-3659	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120823	N/A	ANDA	ANDA090869	Actavis Pharma, Inc.	ROPINIROLE HYDROCHLORIDE	4 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-3659-09)
42291-716-30	42291-716	HUMAN PRESCRIPTION DRUG	Ropinirole Hydrochloride	Ropinirole Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231101	N/A	ANDA	ANDA090869	AvKARE	ROPINIROLE HYDROCHLORIDE	8 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-716-30)
0228-3640-03	0228-3640	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120823	N/A	ANDA	ANDA090869	Actavis Pharma, Inc.	ROPINIROLE HYDROCHLORIDE	6 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-3640-03)
0228-3661-03	0228-3661	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120823	N/A	ANDA	ANDA090869	Actavis Pharma, Inc.	ROPINIROLE HYDROCHLORIDE	12 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-3661-03)
42291-714-30	42291-714	HUMAN PRESCRIPTION DRUG	Ropinirole Hydrochloride	Ropinirole Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231101	N/A	ANDA	ANDA090869	AvKARE	ROPINIROLE HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-714-30)
0228-3660-03	0228-3660	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120823	N/A	ANDA	ANDA090869	Actavis Pharma, Inc.	ROPINIROLE HYDROCHLORIDE	8 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-3660-03)
0228-3660-09	0228-3660	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120823	N/A	ANDA	ANDA090869	Actavis Pharma, Inc.	ROPINIROLE HYDROCHLORIDE	8 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-3660-09)
42291-717-30	42291-717	HUMAN PRESCRIPTION DRUG	Ropinirole Hydrochloride	Ropinirole Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231101	N/A	ANDA	ANDA090869	AvKARE	ROPINIROLE HYDROCHLORIDE	12 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-717-30)
42291-713-30	42291-713	HUMAN PRESCRIPTION DRUG	Ropinirole Hydrochloride	Ropinirole Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231101	N/A	ANDA	ANDA090869	AvKARE	ROPINIROLE HYDROCHLORIDE	2 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-713-30)