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
COUMADIN	009218	005	NDA	WARFARIN SODIUM	TABLET;ORAL	10MG	Yes	No	1954/06/08	Approved Prior to Jan 1, 1982	BRISTOL MYERS SQUIBB	Discontinued
COUMADIN	009218	007	NDA	WARFARIN SODIUM	TABLET;ORAL	5MG	Yes	No	1954/06/08	Approved Prior to Jan 1, 1982	BRISTOL MYERS SQUIBB	Discontinued
COUMADIN	009218	012	NDA	WARFARIN SODIUM	INJECTABLE;INJECTION	75MG/VIAL	No	No	1954/06/08	Approved Prior to Jan 1, 1982	BRISTOL MYERS SQUIBB	Discontinued
COUMADIN	009218	013	NDA	WARFARIN SODIUM	TABLET;ORAL	2MG	Yes	No	1954/06/08	Approved Prior to Jan 1, 1982	BRISTOL MYERS SQUIBB	Discontinued
COUMADIN	009218	016	NDA	WARFARIN SODIUM	TABLET;ORAL	7.5MG	Yes	No	1954/06/08	Approved Prior to Jan 1, 1982	BRISTOL MYERS SQUIBB	Discontinued
COUMADIN	009218	018	NDA	WARFARIN SODIUM	TABLET;ORAL	2.5MG	Yes	No	1954/06/08	Approved Prior to Jan 1, 1982	BRISTOL MYERS SQUIBB	Discontinued
COUMADIN	009218	020	NDA	WARFARIN SODIUM	INJECTABLE;INJECTION	50MG/VIAL	No	No	1954/06/08	Approved Prior to Jan 1, 1982	BRISTOL MYERS SQUIBB	Discontinued
COUMADIN	009218	022	NDA	WARFARIN SODIUM	TABLET;ORAL	1MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1954/06/08	1990/03/01	BRISTOL MYERS SQUIBB	Discontinued
COUMADIN	009218	023	NDA	WARFARIN SODIUM	TABLET;ORAL	4MG	Yes	No	1954/06/08	1993/08/24	BRISTOL MYERS SQUIBB	Discontinued
COUMADIN	009218	024	NDA	WARFARIN SODIUM	INJECTABLE;INJECTION	5MG/VIAL	No	No	1954/06/08	1995/02/07	BRISTOL MYERS SQUIBB	Discontinued
COUMADIN	009218	025	NDA	WARFARIN SODIUM	TABLET;ORAL	3MG	Yes	No	1954/06/08	1996/11/18	BRISTOL MYERS SQUIBB	Discontinued
COUMADIN	009218	026	NDA	WARFARIN SODIUM	TABLET;ORAL	6MG	Yes	No	1954/06/08	1996/11/18	BRISTOL MYERS SQUIBB	Discontinued