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
70518-3482-0	70518-3482	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20220817	N/A	ANDA	ANDA090135	REMEDYREPACK INC.	ROPINIROLE HYDROCHLORIDE	1 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3482-0)
68462-254-01	68462-254	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20100225	N/A	ANDA	ANDA090135	Glenmark Pharmaceuticals Inc., USA	ROPINIROLE HYDROCHLORIDE	.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-254-01)
68462-254-10	68462-254	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20100225	N/A	ANDA	ANDA090135	Glenmark Pharmaceuticals Inc., USA	ROPINIROLE HYDROCHLORIDE	.5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68462-254-10)
68462-254-11	68462-254	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20100225	N/A	ANDA	ANDA090135	Glenmark Pharmaceuticals Inc., USA	ROPINIROLE HYDROCHLORIDE	.5 mg/1	10 BLISTER PACK in 1 CARTON (68462-254-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK
68462-258-01	68462-258	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20100225	N/A	ANDA	ANDA090135	Glenmark Pharmaceuticals Inc., USA	ROPINIROLE HYDROCHLORIDE	4 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-258-01)
68462-258-10	68462-258	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20100225	N/A	ANDA	ANDA090135	Glenmark Pharmaceuticals Inc., USA	ROPINIROLE HYDROCHLORIDE	4 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68462-258-10)
72189-416-30	72189-416	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20230201	N/A	ANDA	ANDA090135	Direct_Rx	ROPINIROLE HYDROCHLORIDE	.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-416-30)
70518-3478-0	70518-3478	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20220817	N/A	ANDA	ANDA090135	REMEDYREPACK INC.	ROPINIROLE HYDROCHLORIDE	.5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3478-0)
70518-3478-1	70518-3478	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA090135	REMEDYREPACK INC.	ROPINIROLE HYDROCHLORIDE	.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3478-1)
70518-3478-2	70518-3478	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20250618	N/A	ANDA	ANDA090135	REMEDYREPACK INC.	ROPINIROLE HYDROCHLORIDE	.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3478-2)
70518-3478-3	70518-3478	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20260309	N/A	ANDA	ANDA090135	REMEDYREPACK INC.	ROPINIROLE HYDROCHLORIDE	.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3478-3)
68462-253-01	68462-253	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20100225	N/A	ANDA	ANDA090135	Glenmark Pharmaceuticals Inc., USA	ROPINIROLE HYDROCHLORIDE	.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-253-01)
68462-253-10	68462-253	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20100225	N/A	ANDA	ANDA090135	Glenmark Pharmaceuticals Inc., USA	ROPINIROLE HYDROCHLORIDE	.25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68462-253-10)
68462-253-11	68462-253	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20100225	N/A	ANDA	ANDA090135	Glenmark Pharmaceuticals Inc., USA	ROPINIROLE HYDROCHLORIDE	.25 mg/1	10 BLISTER PACK in 1 CARTON (68462-253-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK
68462-257-01	68462-257	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20100225	N/A	ANDA	ANDA090135	Glenmark Pharmaceuticals Inc., USA	ROPINIROLE HYDROCHLORIDE	3 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-257-01)
68462-257-10	68462-257	HUMAN PRESCRIPTION DRUG	ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20100225	N/A	ANDA	ANDA090135	Glenmark Pharmaceuticals Inc., USA	ROPINIROLE HYDROCHLORIDE	3 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68462-257-10)