美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=HALOPERIDOL"
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
HALOPERIDOL DECANOATE 216730 001 ANDA HALOPERIDOL DECANOATE INJECTABLE;INJECTION EQ 50MG BASE/ML No No 2023/05/23 2023/05/23 MANKIND PHARMA Prescription
HALOPERIDOL DECANOATE 216730 002 ANDA HALOPERIDOL DECANOATE INJECTABLE;INJECTION EQ 100MG BASE/ML No No 2023/05/23 2023/05/23 MANKIND PHARMA Prescription
HALOPERIDOL 218371 001 ANDA HALOPERIDOL LACTATE CONCENTRATE;ORAL EQ 2MG BASE/ML No No 2024/01/31 2024/01/31 RUBICON Prescription
HALOPERIDOL 216918 001 ANDA HALOPERIDOL TABLET;ORAL 0.5MG No No 2024/04/11 2024/04/11 MANKIND PHARMA Prescription
HALOPERIDOL 216918 002 ANDA HALOPERIDOL TABLET;ORAL 1MG No No 2024/04/11 2024/04/11 MANKIND PHARMA Prescription
HALOPERIDOL 216918 003 ANDA HALOPERIDOL TABLET;ORAL 2MG No No 2024/04/11 2024/04/11 MANKIND PHARMA Prescription
HALOPERIDOL 216918 004 ANDA HALOPERIDOL TABLET;ORAL 5MG No No 2024/04/11 2024/04/11 MANKIND PHARMA Prescription
HALOPERIDOL 216918 005 ANDA HALOPERIDOL TABLET;ORAL 10MG No No 2024/04/11 2024/04/11 MANKIND PHARMA Prescription
HALOPERIDOL 216918 006 ANDA HALOPERIDOL TABLET;ORAL 20MG No No 2024/04/11 2024/04/11 MANKIND PHARMA Prescription
HALOPERIDOL 218789 001 ANDA HALOPERIDOL TABLET;ORAL 0.5MG No No 2024/04/19 2024/04/19 AUROBINDO PHARMA LTD Prescription
HALOPERIDOL 218789 002 ANDA HALOPERIDOL TABLET;ORAL 1MG No No 2024/04/19 2024/04/19 AUROBINDO PHARMA LTD Prescription
HALOPERIDOL 218789 003 ANDA HALOPERIDOL TABLET;ORAL 2MG No No 2024/04/19 2024/04/19 AUROBINDO PHARMA LTD Prescription
HALOPERIDOL 218789 004 ANDA HALOPERIDOL TABLET;ORAL 5MG No No 2024/04/19 2024/04/19 AUROBINDO PHARMA LTD Prescription
HALOPERIDOL 218789 005 ANDA HALOPERIDOL TABLET;ORAL 10MG No No 2024/04/19 2024/04/19 AUROBINDO PHARMA LTD Prescription
HALOPERIDOL 218789 006 ANDA HALOPERIDOL TABLET;ORAL 20MG No No 2024/04/19 2024/04/19 AUROBINDO PHARMA LTD Prescription
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