美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=TOPIRAMATE"
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
TOPIRAMATE 217869 001 ANDA TOPIRAMATE CAPSULE;ORAL 15MG No No 2024/07/16 2024/07/16 GLENMARK PHARMS LTD Prescription
TOPIRAMATE 217869 002 ANDA TOPIRAMATE CAPSULE;ORAL 25MG No No 2024/07/16 2024/07/16 GLENMARK PHARMS LTD Prescription
TOPIRAMATE 218642 001 ANDA TOPIRAMATE CAPSULE;ORAL 15MG No No 2024/10/10 2024/10/10 SENORES PHARMS Prescription
TOPIRAMATE 218642 002 ANDA TOPIRAMATE CAPSULE;ORAL 25MG No No 2024/10/10 2024/10/10 SENORES PHARMS Prescription
TOPIRAMATE 217795 001 ANDA TOPIRAMATE SOLUTION;ORAL 25MG/ML No No 2024/10/31 2024/10/31 ALKEM LABS LTD Prescription
TOPIRAMATE 215638 001 ANDA TOPIRAMATE CAPSULE, EXTENDED RELEASE;ORAL 25MG No No 2024/11/05 2024/11/05 XIAMEN LP PHARM CO Prescription
TOPIRAMATE 215638 002 ANDA TOPIRAMATE CAPSULE, EXTENDED RELEASE;ORAL 50MG No No 2024/11/05 2024/11/05 XIAMEN LP PHARM CO Prescription
TOPIRAMATE 215638 003 ANDA TOPIRAMATE CAPSULE, EXTENDED RELEASE;ORAL 100MG No No 2024/11/05 2024/11/05 XIAMEN LP PHARM CO Prescription
TOPIRAMATE 215638 004 ANDA TOPIRAMATE CAPSULE, EXTENDED RELEASE;ORAL 150MG No No 2024/11/05 2024/11/05 XIAMEN LP PHARM CO Prescription
TOPIRAMATE 215638 005 ANDA TOPIRAMATE CAPSULE, EXTENDED RELEASE;ORAL 200MG No No 2024/11/05 2024/11/05 XIAMEN LP PHARM CO Prescription
TOPIRAMATE 218695 001 ANDA TOPIRAMATE CAPSULE, EXTENDED RELEASE;ORAL 25MG No No 2024/12/03 2024/12/03 AMTA Prescription
TOPIRAMATE 218695 002 ANDA TOPIRAMATE CAPSULE, EXTENDED RELEASE;ORAL 50MG No No 2024/12/03 2024/12/03 AMTA Prescription
TOPIRAMATE 218695 003 ANDA TOPIRAMATE CAPSULE, EXTENDED RELEASE;ORAL 100MG No No 2024/12/03 2024/12/03 AMTA Prescription
TOPIRAMATE 218695 004 ANDA TOPIRAMATE CAPSULE, EXTENDED RELEASE;ORAL 150MG No No 2024/12/03 2024/12/03 AMTA Prescription
TOPIRAMATE 218695 005 ANDA TOPIRAMATE CAPSULE, EXTENDED RELEASE;ORAL 200MG No No 2024/12/03 2024/12/03 AMTA Prescription
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