美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=DURICEF"
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
DURICEF 050512 001 NDA CEFADROXIL/CEFADROXIL HEMIHYDRATE CAPSULE;ORAL EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1978/02/17 Approved Prior to Jan 1, 1982 WARNER CHILCOTT Discontinued
DURICEF 050512 002 NDA CEFADROXIL/CEFADROXIL HEMIHYDRATE CAPSULE;ORAL EQ 250MG BASE No No 1978/02/17 Approved Prior to Jan 1, 1982 WARNER CHILCOTT Discontinued
DURICEF 050528 001 NDA CEFADROXIL/CEFADROXIL HEMIHYDRATE TABLET;ORAL EQ 1GM BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1980/08/06 Approved Prior to Jan 1, 1982 WARNER CHILCOTT Discontinued
DURICEF 050527 001 NDA CEFADROXIL/CEFADROXIL HEMIHYDRATE FOR SUSPENSION;ORAL EQ 500MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1980/09/12 Approved Prior to Jan 1, 1982 WARNER CHILCOTT Discontinued
DURICEF 050527 002 NDA CEFADROXIL/CEFADROXIL HEMIHYDRATE FOR SUSPENSION;ORAL EQ 125MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1980/09/12 Approved Prior to Jan 1, 1982 WARNER CHILCOTT Discontinued
DURICEF 050527 003 NDA CEFADROXIL/CEFADROXIL HEMIHYDRATE FOR SUSPENSION;ORAL EQ 250MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1980/09/12 Approved Prior to Jan 1, 1982 WARNER CHILCOTT Discontinued
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