美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=ACIPHEX"
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
ACIPHEX 020973 001 NDA RABEPRAZOLE SODIUM TABLET, DELAYED RELEASE;ORAL 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1999/08/19 2002/05/29 EISAI INC Discontinued
ACIPHEX 020973 002 NDA RABEPRAZOLE SODIUM TABLET, DELAYED RELEASE;ORAL 20MG Yes Yes 1999/08/19 1999/08/19 EISAI INC Prescription
ACIPHEX 021456 001 NDA RABEPRAZOLE SODIUM Tablet, Delayed Release; Oral 20MG No 2002/11/08 EISAI MEDCL RES Prescription
ACIPHEX SPRINKLE 204736 001 NDA RABEPRAZOLE SODIUM CAPSULE, DELAYED RELEASE;ORAL 5MG Yes No 2013/03/26 2013/03/26 CERECOR INC Prescription
ACIPHEX SPRINKLE 204736 002 NDA RABEPRAZOLE SODIUM CAPSULE, DELAYED RELEASE;ORAL 10MG Yes Yes 2013/03/26 2013/03/26 CERECOR INC Prescription
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