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
10135-676-01	10135-676	HUMAN PRESCRIPTION DRUG	Ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20190315	N/A	ANDA	ANDA079165	Marlex Pharmaceuticals Inc	ROPINIROLE HYDROCHLORIDE	2 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (10135-676-01)
10135-677-01	10135-677	HUMAN PRESCRIPTION DRUG	Ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20190315	N/A	ANDA	ANDA079165	Marlex Pharmaceuticals Inc	ROPINIROLE HYDROCHLORIDE	3 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (10135-677-01)
10135-678-01	10135-678	HUMAN PRESCRIPTION DRUG	Ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20190315	N/A	ANDA	ANDA079165	Marlex Pharmaceuticals Inc	ROPINIROLE HYDROCHLORIDE	4 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (10135-678-01)
10135-679-01	10135-679	HUMAN PRESCRIPTION DRUG	Ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20190315	N/A	ANDA	ANDA079165	Marlex Pharmaceuticals Inc	ROPINIROLE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (10135-679-01)
10135-675-01	10135-675	HUMAN PRESCRIPTION DRUG	Ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20190315	N/A	ANDA	ANDA079165	Marlex Pharmaceuticals Inc	ROPINIROLE HYDROCHLORIDE	1 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (10135-675-01)
10135-674-01	10135-674	HUMAN PRESCRIPTION DRUG	Ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20190315	N/A	ANDA	ANDA079165	Marlex Pharmaceuticals Inc	ROPINIROLE HYDROCHLORIDE	.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (10135-674-01)
10135-673-01	10135-673	HUMAN PRESCRIPTION DRUG	Ropinirole	ropinirole	TABLET, FILM COATED	ORAL	20190315	N/A	ANDA	ANDA079165	Marlex Pharmaceuticals Inc	ROPINIROLE HYDROCHLORIDE	.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (10135-673-01)