美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=PHENYTOIN"
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
EXTENDED PHENYTOIN SODIUM 040731 002 ANDA PHENYTOIN SODIUM CAPSULE;ORAL 300MG EXTENDED No No 2008/06/30 2008/06/30 SUN PHARM INDS Discontinued
EXTENDED PHENYTOIN SODIUM 040765 001 ANDA PHENYTOIN SODIUM CAPSULE;ORAL 100MG EXTENDED No No 2008/11/12 2008/11/12 AMNEAL PHARMS NY Prescription
FOSPHENYTOIN SODIUM 078765 001 ANDA FOSPHENYTOIN SODIUM INJECTABLE;INJECTION EQ 50MG PHENYTOIN NA/ML No No 2009/12/02 2009/12/02 HIKMA FARMACEUTICA Prescription
FOSPHENYTOIN SODIUM 090099 001 ANDA FOSPHENYTOIN SODIUM INJECTABLE;INJECTION EQ 50MG PHENYTOIN NA/ML No No 2010/05/13 2010/05/13 AM REGENT Discontinued
FOSPHENYTOIN SODIUM 078736 001 ANDA FOSPHENYTOIN SODIUM INJECTABLE;INJECTION EQ 50MG PHENYTOIN NA/ML No No 2010/06/08 2010/06/08 NORVIUM BIOSCIENCE Discontinued
PHENYTOIN 200691 001 ANDA PHENYTOIN TABLET, CHEWABLE;ORAL 50MG No No 2012/12/26 2012/12/26 RISING Prescription
PHENYTOIN 200565 001 ANDA PHENYTOIN TABLET, CHEWABLE;ORAL 50MG No No 2014/04/17 2014/04/17 TARO Prescription
PHENYTOIN 040884 001 ANDA PHENYTOIN TABLET, CHEWABLE;ORAL 50MG No No 2014/11/28 2014/11/28 EPIC PHARMA LLC Prescription
PHENYTOIN SODIUM 204309 001 ANDA PHENYTOIN SODIUM CAPSULE;ORAL 100MG EXTENDED No No 2015/06/10 2015/06/10 AUROBINDO PHARMA Prescription
EXTENDED PHENYTOIN SODIUM 211633 001 ANDA PHENYTOIN SODIUM CAPSULE;ORAL 100MG EXTENDED No No 2019/09/30 2019/09/30 LUPIN LTD Discontinued
EXTENDED PHENYTOIN SODIUM 213834 001 ANDA PHENYTOIN SODIUM CAPSULE;ORAL 100MG EXTENDED No No 2022/10/13 2022/10/13 UNICHEM Discontinued
FOSPHENYTOIN SODIUM 214926 001 ANDA FOSPHENYTOIN SODIUM INJECTABLE;INJECTION EQ 50MG PHENYTOIN NA/ML No No 2023/10/13 2023/10/13 GLAND PHARMA LTD Prescription
药品名称,活性成分,申请号搜索 高级检索
©2006-2024 DrugFuture->U.S. FDA Drugs Database