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
PRAVACHOL	019898	002	NDA	PRAVASTATIN SODIUM	TABLET;ORAL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1991/10/31	1991/10/31	BRISTOL MYERS SQUIBB	Discontinued
PRAVACHOL	019898	003	NDA	PRAVASTATIN SODIUM	TABLET;ORAL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1991/10/31	1991/10/31	BRISTOL MYERS SQUIBB	Discontinued
PRAVACHOL	019898	004	NDA	PRAVASTATIN SODIUM	TABLET;ORAL	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1991/10/31	1993/03/22	BRISTOL MYERS SQUIBB	Discontinued
PRAVACHOL	019898	008	NDA	PRAVASTATIN SODIUM	TABLET;ORAL	80MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1991/10/31	2001/12/18	BRISTOL MYERS SQUIBB	Discontinued