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
71335-1231-4	71335-1231	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20241031	N/A	ANDA	ANDA204022	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-1231-4)
71335-1188-2	71335-1188	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20190412	N/A	ANDA	ANDA204022	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1188-2)
71335-1188-3	71335-1188	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20241031	N/A	ANDA	ANDA204022	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1188-3)
71335-1188-4	71335-1188	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20241031	N/A	ANDA	ANDA204022	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	.5 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (71335-1188-4)
72189-222-30	72189-222	HUMAN PRESCRIPTION DRUG	ROPINIROLE	ROPINIROLE	TABLET, FILM COATED	ORAL	20210520	N/A	ANDA	ANDA204022	DIRECT RX	ROPINIROLE HYDROCHLORIDE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-222-30)
72189-222-60	72189-222	HUMAN PRESCRIPTION DRUG	ROPINIROLE	ROPINIROLE	TABLET, FILM COATED	ORAL	20210520	N/A	ANDA	ANDA204022	DIRECT RX	ROPINIROLE HYDROCHLORIDE	1 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72189-222-60)
72189-364-30	72189-364	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20220621	N/A	ANDA	ANDA204022	Direct_Rx	ROPINIROLE HYDROCHLORIDE	.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-364-30)