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
MEXITIL	018873	002	NDA	MEXILETINE HYDROCHLORIDE	CAPSULE;ORAL	150MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1985/12/30	1985/12/30	BOEHRINGER INGELHEIM	Discontinued
MEXITIL	018873	003	NDA	MEXILETINE HYDROCHLORIDE	CAPSULE;ORAL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1985/12/30	1985/12/30	BOEHRINGER INGELHEIM	Discontinued
MEXITIL	018873	004	NDA	MEXILETINE HYDROCHLORIDE	CAPSULE;ORAL	250MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1985/12/30	1985/12/30	BOEHRINGER INGELHEIM	Discontinued