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
71335-1434-3	71335-1434	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20191212	N/A	ANDA	ANDA078110	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	1 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1434-3)
71335-1434-4	71335-1434	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20191212	N/A	ANDA	ANDA078110	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	1 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1434-4)
50090-4348-0	50090-4348	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20190611	N/A	ANDA	ANDA078110	A-S Medication Solutions	ROPINIROLE HYDROCHLORIDE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-4348-0)
50090-4348-1	50090-4348	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20190611	N/A	ANDA	ANDA078110	A-S Medication Solutions	ROPINIROLE HYDROCHLORIDE	1 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-4348-1)
71335-1626-1	71335-1626	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20200608	N/A	ANDA	ANDA078110	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	2 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1626-1)
71335-1626-2	71335-1626	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20200608	N/A	ANDA	ANDA078110	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	2 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1626-2)
71335-1626-3	71335-1626	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20200608	N/A	ANDA	ANDA078110	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	2 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1626-3)
51655-360-26	51655-360	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20200528	N/A	ANDA	ANDA078110	Northwind Pharmaceuticals, LLC	ROPINIROLE HYDROCHLORIDE	.25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-360-26)
60687-577-01	60687-577	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20210610	N/A	ANDA	ANDA078110	American Health Packaging	ROPINIROLE HYDROCHLORIDE	.25 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-577-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-577-11)
60687-588-01	60687-588	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20210609	N/A	ANDA	ANDA078110	American Health Packaging	ROPINIROLE HYDROCHLORIDE	1 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-588-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-588-11)
71205-825-30	71205-825	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20230811	N/A	ANDA	ANDA078110	Proficient Rx LP	ROPINIROLE HYDROCHLORIDE	.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-825-30)
71205-825-60	71205-825	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20230811	N/A	ANDA	ANDA078110	Proficient Rx LP	ROPINIROLE HYDROCHLORIDE	.25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-825-60)
71205-825-90	71205-825	HUMAN PRESCRIPTION DRUG	ropinirole hydrochloride	ropinirole hydrochloride	TABLET, FILM COATED	ORAL	20230811	N/A	ANDA	ANDA078110	Proficient Rx LP	ROPINIROLE HYDROCHLORIDE	.25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-825-90)