美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=RABEPRAZOLE SODIUM"
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
RABEPRAZOLE SODIUM 076822 001 ANDA RABEPRAZOLE SODIUM TABLET, DELAYED RELEASE;ORAL 20MG No No 2013/11/08 2013/11/08 TEVA PHARMS USA Prescription
RABEPRAZOLE SODIUM 076824 001 ANDA RABEPRAZOLE SODIUM TABLET, DELAYED RELEASE;ORAL 20MG No No 2013/11/08 2013/11/08 DR REDDYS Prescription
RABEPRAZOLE SODIUM 076885 001 ANDA RABEPRAZOLE SODIUM TABLET, DELAYED RELEASE;ORAL 20MG No No 2013/11/08 2013/11/08 MYLAN Discontinued
RABEPRAZOLE SODIUM 078964 001 ANDA RABEPRAZOLE SODIUM TABLET, DELAYED RELEASE;ORAL 20MG No No 2013/11/08 2013/11/08 LUPIN LTD Prescription
RABEPRAZOLE SODIUM 090678 001 ANDA RABEPRAZOLE SODIUM TABLET, DELAYED RELEASE;ORAL 20MG No No 2013/11/08 2013/11/08 LANNETT CO INC Prescription
RABEPRAZOLE SODIUM 202376 001 ANDA RABEPRAZOLE SODIUM TABLET, DELAYED RELEASE;ORAL 20MG No No 2013/11/08 2013/11/08 TORRENT Prescription
RABEPRAZOLE SODIUM 204179 001 ANDA RABEPRAZOLE SODIUM TABLET, DELAYED RELEASE;ORAL 20MG No No 2015/07/31 2015/07/31 AMNEAL PHARMS Prescription
RABEPRAZOLE SODIUM 204237 001 ANDA RABEPRAZOLE SODIUM TABLET, DELAYED RELEASE;ORAL 20MG No No 2015/11/18 2015/11/18 RUBICON Prescription
RABEPRAZOLE SODIUM 205761 001 ANDA RABEPRAZOLE SODIUM TABLET, DELAYED RELEASE;ORAL 20MG No No 2017/02/17 2017/02/17 AUROBINDO PHARMA LTD Prescription
RABEPRAZOLE SODIUM 208644 001 ANDA RABEPRAZOLE SODIUM TABLET, DELAYED RELEASE;ORAL 20MG No No 2018/04/24 2018/04/24 ALKEM LABS LTD Prescription
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