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
SULAR	020356	001	NDA	NISOLDIPINE	TABLET, EXTENDED RELEASE;ORAL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1995/02/02	1995/02/02	COVIS	Discontinued
SULAR	020356	002	NDA	NISOLDIPINE	TABLET, EXTENDED RELEASE;ORAL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1995/02/02	1995/02/02	COVIS	Discontinued
SULAR	020356	003	NDA	NISOLDIPINE	TABLET, EXTENDED RELEASE;ORAL	30MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1995/02/02	1995/02/02	COVIS	Discontinued
SULAR	020356	004	NDA	NISOLDIPINE	TABLET, EXTENDED RELEASE;ORAL	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1995/02/02	1995/02/02	COVIS	Discontinued
SULAR	020356	005	NDA	NISOLDIPINE	TABLET, EXTENDED RELEASE;ORAL	34MG	Yes	Yes	1995/02/02	2008/01/02	COVIS	Prescription
SULAR	020356	006	NDA	NISOLDIPINE	TABLET, EXTENDED RELEASE;ORAL	25.5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1995/02/02	2008/01/02	COVIS	Discontinued
SULAR	020356	007	NDA	NISOLDIPINE	TABLET, EXTENDED RELEASE;ORAL	17MG	Yes	Yes	1995/02/02	2008/01/02	COVIS	Prescription
SULAR	020356	008	NDA	NISOLDIPINE	TABLET, EXTENDED RELEASE;ORAL	8.5MG	Yes	Yes	1995/02/02	2008/01/02	COVIS	Prescription