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
55154-7888-0	55154-7888	HUMAN PRESCRIPTION DRUG	ROPINIROLE HYDROCHLORIDE	ROPINIROLE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141001	N/A	ANDA	ANDA090429	Cardinal Health 107, LLC	ROPINIROLE HYDROCHLORIDE	.25 mg/1	10 BLISTER PACK in 1 BAG (55154-7888-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0615-8190-39	0615-8190	HUMAN PRESCRIPTION DRUG	ROPINIROLE HYDROCHLORIDE	ROPINIROLE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20180307	N/A	ANDA	ANDA090429	NCS HealthCare of KY, Inc dba Vangard Labs	ROPINIROLE HYDROCHLORIDE	1 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8190-39)
0615-8191-39	0615-8191	HUMAN PRESCRIPTION DRUG	ROPINIROLE HYDROCHLORIDE	ROPINIROLE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20180305	N/A	ANDA	ANDA090429	NCS HealthCare of KY, Inc dba Vangard Labs	ROPINIROLE HYDROCHLORIDE	2 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8191-39)
0615-8189-39	0615-8189	HUMAN PRESCRIPTION DRUG	ROPINIROLE HYDROCHLORIDE	ROPINIROLE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20180306	N/A	ANDA	ANDA090429	NCS HealthCare of KY, Inc dba Vangard Labs	ROPINIROLE HYDROCHLORIDE	.5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8189-39)
0615-8188-39	0615-8188	HUMAN PRESCRIPTION DRUG	ROPINIROLE HYDROCHLORIDE	ROPINIROLE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20180305	N/A	ANDA	ANDA090429	NCS HealthCare of KY, Inc dba Vangard Labs	ROPINIROLE HYDROCHLORIDE	.25 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8188-39)
55154-7633-0	55154-7633	HUMAN PRESCRIPTION DRUG	ROPINIROLE HYDROCHLORIDE	ROPINIROLE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20141001	N/A	ANDA	ANDA090429	Cardinal Health 107, LLC	ROPINIROLE HYDROCHLORIDE	1 mg/1	10 BLISTER PACK in 1 BAG (55154-7633-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
46708-031-31	46708-031	HUMAN PRESCRIPTION DRUG	ROPINIROLE HYDROCHLORIDE	ROPINIROLE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20130912	N/A	ANDA	ANDA090429	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (46708-031-31)
46708-032-30	46708-032	HUMAN PRESCRIPTION DRUG	ROPINIROLE HYDROCHLORIDE	ROPINIROLE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20130912	N/A	ANDA	ANDA090429	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (46708-032-30)
46708-032-31	46708-032	HUMAN PRESCRIPTION DRUG	ROPINIROLE HYDROCHLORIDE	ROPINIROLE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20130912	N/A	ANDA	ANDA090429	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	1 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (46708-032-31)
46708-030-30	46708-030	HUMAN PRESCRIPTION DRUG	ROPINIROLE HYDROCHLORIDE	ROPINIROLE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20130912	N/A	ANDA	ANDA090429	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (46708-030-30)
46708-030-31	46708-030	HUMAN PRESCRIPTION DRUG	ROPINIROLE HYDROCHLORIDE	ROPINIROLE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20130912	N/A	ANDA	ANDA090429	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (46708-030-31)
46708-033-30	46708-033	HUMAN PRESCRIPTION DRUG	ROPINIROLE HYDROCHLORIDE	ROPINIROLE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20130912	N/A	ANDA	ANDA090429	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	2 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (46708-033-30)
46708-033-31	46708-033	HUMAN PRESCRIPTION DRUG	ROPINIROLE HYDROCHLORIDE	ROPINIROLE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20130912	N/A	ANDA	ANDA090429	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	2 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (46708-033-31)
46708-034-30	46708-034	HUMAN PRESCRIPTION DRUG	ROPINIROLE HYDROCHLORIDE	ROPINIROLE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20130912	N/A	ANDA	ANDA090429	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	3 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (46708-034-30)
46708-034-31	46708-034	HUMAN PRESCRIPTION DRUG	ROPINIROLE HYDROCHLORIDE	ROPINIROLE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20130912	N/A	ANDA	ANDA090429	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	3 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (46708-034-31)
46708-035-30	46708-035	HUMAN PRESCRIPTION DRUG	ROPINIROLE HYDROCHLORIDE	ROPINIROLE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20130912	N/A	ANDA	ANDA090429	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (46708-035-30)
46708-035-31	46708-035	HUMAN PRESCRIPTION DRUG	ROPINIROLE HYDROCHLORIDE	ROPINIROLE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20130912	N/A	ANDA	ANDA090429	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	4 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (46708-035-31)
46708-036-30	46708-036	HUMAN PRESCRIPTION DRUG	ROPINIROLE HYDROCHLORIDE	ROPINIROLE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20130912	N/A	ANDA	ANDA090429	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (46708-036-30)
46708-036-31	46708-036	HUMAN PRESCRIPTION DRUG	ROPINIROLE HYDROCHLORIDE	ROPINIROLE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20130912	N/A	ANDA	ANDA090429	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (46708-036-31)
46708-031-30	46708-031	HUMAN PRESCRIPTION DRUG	ROPINIROLE HYDROCHLORIDE	ROPINIROLE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20130912	N/A	ANDA	ANDA090429	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (46708-031-30)