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
46708-262-71	46708-262	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130314	N/A	ANDA	ANDA202786	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	2 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-262-71)
46708-262-90	46708-262	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130314	N/A	ANDA	ANDA202786	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	2 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-262-90)
46708-262-91	46708-262	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130314	N/A	ANDA	ANDA202786	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	2 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-262-91)
46708-263-10	46708-263	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130314	N/A	ANDA	ANDA202786	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	4 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (46708-263-10)
46708-263-30	46708-263	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130314	N/A	ANDA	ANDA202786	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-263-30)
46708-263-31	46708-263	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130314	N/A	ANDA	ANDA202786	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	4 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-263-31)
46708-263-71	46708-263	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130314	N/A	ANDA	ANDA202786	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	4 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-263-71)
46708-263-90	46708-263	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130314	N/A	ANDA	ANDA202786	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	4 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-263-90)
46708-263-91	46708-263	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130314	N/A	ANDA	ANDA202786	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	4 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-263-91)
46708-264-10	46708-264	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130314	N/A	ANDA	ANDA202786	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	6 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (46708-264-10)
46708-262-31	46708-262	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130314	N/A	ANDA	ANDA202786	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	2 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-262-31)
46708-262-30	46708-262	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130314	N/A	ANDA	ANDA202786	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	2 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-262-30)
46708-262-10	46708-262	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130314	N/A	ANDA	ANDA202786	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	2 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (46708-262-10)
46708-264-30	46708-264	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130314	N/A	ANDA	ANDA202786	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	6 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-264-30)
46708-264-91	46708-264	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130314	N/A	ANDA	ANDA202786	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	6 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-264-91)
46708-265-10	46708-265	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130314	N/A	ANDA	ANDA202786	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	8 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (46708-265-10)
46708-265-30	46708-265	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130314	N/A	ANDA	ANDA202786	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	8 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-265-30)
46708-265-31	46708-265	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130314	N/A	ANDA	ANDA202786	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	8 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-265-31)
46708-265-71	46708-265	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130314	N/A	ANDA	ANDA202786	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	8 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-265-71)
46708-265-90	46708-265	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130314	N/A	ANDA	ANDA202786	Alembic Pharmaceuticals Limited	ROPINIROLE HYDROCHLORIDE	8 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-265-90)