美国FDA药品数据库-药物在线

商品名	申请号	产品号	申请类型	活性成分	剂型/给药途径	规格/剂量	RLD	RS	申请号原始批准/暂定批准日期	产品号批准日期	申请人	市场状态
CHOLEDYL	009268	003	NDA	OXTRIPHYLLINE	TABLET, DELAYED RELEASE;ORAL	100MG	No	No	--	Approved Prior to Jan 1, 1982	PARKE DAVIS	Discontinued
CHOLEDYL	009268	007	NDA	OXTRIPHYLLINE	TABLET, DELAYED RELEASE;ORAL	200MG	No	No	--	Approved Prior to Jan 1, 1982	PARKE DAVIS	Discontinued
CHOLEDYL	009268	011	NDA	OXTRIPHYLLINE	SYRUP;ORAL	50MG/5ML	No	No	--	Approved Prior to Jan 1, 1982	PARKE DAVIS	Discontinued
CHOLEDYL	009268	012	NDA	OXTRIPHYLLINE	SOLUTION;ORAL	100MG/5ML	No	No	--	1984/11/27	PARKE DAVIS	Discontinued
CHOLEDYL SA	086742	001	ANDA	OXTRIPHYLLINE	TABLET, EXTENDED RELEASE;ORAL	600MG	No	No	1981/11/05	Approved Prior to Jan 1, 1982	WARNER CHILCOTT LLC	Discontinued
CHOLEDYL SA	087863	001	ANDA	OXTRIPHYLLINE	TABLET, EXTENDED RELEASE;ORAL	400MG	No	No	1983/05/24	1983/05/24	WARNER CHILCOTT LLC	Discontinued