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
EVEKEO	200166	001	ANDA	AMPHETAMINE SULFATE	TABLET;ORAL	5MG	No	No	2012/08/09	2012/08/09	AZURITY	Prescription
EVEKEO	200166	002	ANDA	AMPHETAMINE SULFATE	TABLET;ORAL	10MG	No	Yes	2012/08/09	2012/08/09	AZURITY	Prescription
EVEKEO ODT	209905	001	NDA	AMPHETAMINE SULFATE	TABLET, ORALLY DISINTEGRATING;ORAL	5MG	Yes	No	2019/01/30	2019/01/30	AZURITY	Discontinued
EVEKEO ODT	209905	002	NDA	AMPHETAMINE SULFATE	TABLET, ORALLY DISINTEGRATING;ORAL	10MG	Yes	No	2019/01/30	2019/01/30	AZURITY	Discontinued
EVEKEO ODT	209905	003	NDA	AMPHETAMINE SULFATE	TABLET, ORALLY DISINTEGRATING;ORAL	15MG	Yes	No	2019/01/30	2019/01/30	AZURITY	Discontinued
EVEKEO ODT	209905	004	NDA	AMPHETAMINE SULFATE	TABLET, ORALLY DISINTEGRATING;ORAL	20MG	Yes	No	2019/01/30	2019/01/30	AZURITY	Discontinued
EVEKEO ODT	209905	005	NDA	AMPHETAMINE SULFATE	TABLET, ORALLY DISINTEGRATING;ORAL	2.5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	2019/01/30	2021/04/16	AZURITY	Discontinued