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
DALFAMPRIDINE	206854	001	ANDA	DALFAMPRIDINE	TABLET, EXTENDED RELEASE;ORAL	10MG	No	No	2016/07/19 (TA)	--	TEVA PHARMS USA INC	None (Tentative Approval)
DALFAMPRIDINE	206811	001	ANDA	DALFAMPRIDINE	TABLET, EXTENDED RELEASE;ORAL	10MG	No	No	2017/01/23	2017/01/23	AUROBINDO PHARMA	Prescription
DALFAMPRIDINE	206836	001	ANDA	DALFAMPRIDINE	TABLET, EXTENDED RELEASE;ORAL	10MG	No	No	2017/01/23	2017/01/23	ACTAVIS LABS FL INC	Prescription
DALFAMPRIDINE	206863	001	ANDA	DALFAMPRIDINE	TABLET, EXTENDED RELEASE;ORAL	10MG	No	No	2018/07/11	2018/07/11	ACCORD HLTHCARE	Prescription
DALFAMPRIDINE	206765	001	ANDA	DALFAMPRIDINE	TABLET, EXTENDED RELEASE;ORAL	10MG	No	No	2018/07/30	2018/07/30	ALKEM LABS LTD	Prescription
DALFAMPRIDINE	206646	001	ANDA	DALFAMPRIDINE	TABLET, EXTENDED RELEASE;ORAL	10MG	No	No	2018/10/24	2018/10/24	HIKMA	Discontinued
DALFAMPRIDINE	210158	001	ANDA	DALFAMPRIDINE	TABLET, EXTENDED RELEASE;ORAL	10MG	No	No	2019/03/11	2019/03/11	MICRO LABS	Prescription
DALFAMPRIDINE	208292	001	ANDA	DALFAMPRIDINE	TABLET, EXTENDED RELEASE;ORAL	10MG	No	No	2019/05/21	2019/05/21	SUN PHARM	Prescription
DALFAMPRIDINE	206858	001	ANDA	DALFAMPRIDINE	TABLET, EXTENDED RELEASE;ORAL	10MG	No	No	2020/07/06	2020/07/06	RISING	Discontinued