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
THEO-DUR	087995	001	ANDA	THEOPHYLLINE	CAPSULE, EXTENDED RELEASE;ORAL	200MG	No	No	--	1985/09/10	SCHERING	Discontinued
THEO-DUR	088015	001	ANDA	THEOPHYLLINE	CAPSULE, EXTENDED RELEASE;ORAL	75MG	No	No	--	1985/09/10	SCHERING	Discontinued
THEO-DUR	088016	001	ANDA	THEOPHYLLINE	CAPSULE, EXTENDED RELEASE;ORAL	125MG	No	No	--	1985/09/10	SCHERING	Discontinued
THEO-DUR	088022	001	ANDA	THEOPHYLLINE	CAPSULE, EXTENDED RELEASE;ORAL	50MG	No	No	--	1985/09/10	SCHERING	Discontinued
THEO-DUR	085328	001	ANDA	THEOPHYLLINE	TABLET, EXTENDED RELEASE;ORAL	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1979/04/12	Approved Prior to Jan 1, 1982	SCHERING	Discontinued
THEO-DUR	085328	002	ANDA	THEOPHYLLINE	TABLET, EXTENDED RELEASE;ORAL	300MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1979/04/12	Approved Prior to Jan 1, 1982	SCHERING	Discontinued
THEO-DUR	086998	001	ANDA	THEOPHYLLINE	TABLET, EXTENDED RELEASE;ORAL	200MG	Yes	No	1980/01/31	Approved Prior to Jan 1, 1982	SCHERING	Discontinued
THEO-DUR	089131	001	ANDA	THEOPHYLLINE	TABLET, EXTENDED RELEASE;ORAL	450MG	No	No	1986/06/25	1986/06/25	SCHERING	Discontinued