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
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)
16729-234-01	16729-234	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20181017	N/A	ANDA	ANDA204022	Accord Healthcare Inc.	ROPINIROLE HYDROCHLORIDE	1 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16729-234-01)
16729-238-01	16729-238	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20181017	N/A	ANDA	ANDA204022	Accord Healthcare Inc.	ROPINIROLE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16729-238-01)
71335-1231-1	71335-1231	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20190524	N/A	ANDA	ANDA204022	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1231-1)
71335-1231-2	71335-1231	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20241031	N/A	ANDA	ANDA204022	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	.25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1231-2)
71335-1231-3	71335-1231	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20241031	N/A	ANDA	ANDA204022	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	.25 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (71335-1231-3)
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)