美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=VANTIN"
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
VANTIN 050674 001 NDA CEFPODOXIME PROXETIL TABLET;ORAL EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1992/08/07 1992/08/07 PHARMACIA AND UPJOHN Discontinued
VANTIN 050674 002 NDA CEFPODOXIME PROXETIL TABLET;ORAL EQ 200MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1992/08/07 1992/08/07 PHARMACIA AND UPJOHN Discontinued
VANTIN 050675 001 NDA CEFPODOXIME PROXETIL FOR SUSPENSION;ORAL EQ 50MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1992/08/07 1992/08/07 PHARMACIA AND UPJOHN Discontinued
VANTIN 050675 002 NDA CEFPODOXIME PROXETIL FOR SUSPENSION;ORAL EQ 100MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1992/08/07 1992/08/07 PHARMACIA AND UPJOHN Discontinued
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