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
68462-253-01	68462-253	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20100225	N/A	ANDA	ANDA090135	Glenmark Pharmaceuticals Inc., USA	ROPINIROLE HYDROCHLORIDE	.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-253-01)
68462-259-01	68462-259	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20100225	N/A	ANDA	ANDA090135	Glenmark Pharmaceuticals Inc., USA	ROPINIROLE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-259-01)
68462-259-10	68462-259	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20100225	N/A	ANDA	ANDA090135	Glenmark Pharmaceuticals Inc., USA	ROPINIROLE HYDROCHLORIDE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68462-259-10)
68462-259-11	68462-259	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20100225	N/A	ANDA	ANDA090135	Glenmark Pharmaceuticals Inc., USA	ROPINIROLE HYDROCHLORIDE	5 mg/1	10 BLISTER PACK in 1 CARTON (68462-259-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK
68462-253-10	68462-253	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20100225	N/A	ANDA	ANDA090135	Glenmark Pharmaceuticals Inc., USA	ROPINIROLE HYDROCHLORIDE	.25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68462-253-10)
68462-258-10	68462-258	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20100225	N/A	ANDA	ANDA090135	Glenmark Pharmaceuticals Inc., USA	ROPINIROLE HYDROCHLORIDE	4 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68462-258-10)
68462-258-01	68462-258	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20100225	N/A	ANDA	ANDA090135	Glenmark Pharmaceuticals Inc., USA	ROPINIROLE HYDROCHLORIDE	4 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-258-01)
50090-4684-0	50090-4684	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20191105	N/A	ANDA	ANDA090135	A-S Medication Solutions	ROPINIROLE HYDROCHLORIDE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-4684-0)
50090-4684-1	50090-4684	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20191105	N/A	ANDA	ANDA090135	A-S Medication Solutions	ROPINIROLE HYDROCHLORIDE	1 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-4684-1)
71335-0447-1	71335-0447	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20240524	N/A	ANDA	ANDA090135	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0447-1)
71335-0447-2	71335-0447	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20240524	N/A	ANDA	ANDA090135	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	1 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (71335-0447-2)
71335-0447-3	71335-0447	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20240524	N/A	ANDA	ANDA090135	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	1 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0447-3)
71335-0447-4	71335-0447	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20240524	N/A	ANDA	ANDA090135	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	1 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0447-4)
71335-0631-1	71335-0631	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20240524	N/A	ANDA	ANDA090135	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	2 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0631-1)
71335-0631-2	71335-0631	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20240524	N/A	ANDA	ANDA090135	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	2 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0631-2)
71335-0631-3	71335-0631	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20240524	N/A	ANDA	ANDA090135	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	2 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0631-3)