美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=DALFAMPRIDINE"
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 2016/07/19 (TA) TEVA PHARMS USA INC None (Tentative Approval)
DALFAMPRIDINE 206858 001 ANDA DALFAMPRIDINE TABLET, EXTENDED RELEASE;ORAL 10MG No 2016/09/14 (TA) MYLAN PHARMS INC None (Tentative Approval)
DALFAMPRIDINE 206811 001 ANDA DALFAMPRIDINE TABLET, EXTENDED RELEASE;ORAL 10MG No No 2017/01/23 2017/01/23 AUROBINDO PHARMA LTD 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 Prescription
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
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