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
71335-2515-2	71335-2515	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20241024	N/A	ANDA	ANDA079229	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	2 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2515-2)
71335-2515-3	71335-2515	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20241024	N/A	ANDA	ANDA079229	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	2 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2515-3)
69452-357-20	69452-357	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20220915	N/A	ANDA	ANDA079229	Bionpharma Inc.	ROPINIROLE HYDROCHLORIDE	.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-357-20)
69452-361-20	69452-361	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20220915	N/A	ANDA	ANDA079229	Bionpharma Inc.	ROPINIROLE HYDROCHLORIDE	4 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-361-20)