美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=SUPRENZA"
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
SUPRENZA 202088 001 NDA PHENTERMINE HYDROCHLORIDE TABLET, ORALLY DISINTEGRATING;ORAL 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** No No 2011/06/13 2011/06/13 CITIUS PHARMS Discontinued
SUPRENZA 202088 002 NDA PHENTERMINE HYDROCHLORIDE TABLET, ORALLY DISINTEGRATING;ORAL 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** No No 2011/06/13 2011/06/13 CITIUS PHARMS Discontinued
SUPRENZA 202088 003 NDA PHENTERMINE HYDROCHLORIDE TABLET, ORALLY DISINTEGRATING;ORAL 37.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** No No 2011/06/13 2012/03/27 CITIUS PHARMS Discontinued
SUPRENZA 202088 001 NDA PHENTERMINE HYDROCHLORIDE TABLET, ORALLY DISINTEGRATING;ORAL 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** No No 2012/03/27 2011/06/13 CITIUS PHARMS Discontinued
SUPRENZA 202088 002 NDA PHENTERMINE HYDROCHLORIDE TABLET, ORALLY DISINTEGRATING;ORAL 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** No No 2012/03/27 2011/06/13 CITIUS PHARMS Discontinued
SUPRENZA 202088 003 NDA PHENTERMINE HYDROCHLORIDE TABLET, ORALLY DISINTEGRATING;ORAL 37.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** No No 2012/03/27 2012/03/27 CITIUS PHARMS Discontinued
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