美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=CECLOR"
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
CECLOR 050521 001 NDA CEFACLOR CAPSULE;ORAL EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1979/04/04 Approved Prior to Jan 1, 1982 LILLY Discontinued
CECLOR 050521 002 NDA CEFACLOR CAPSULE;ORAL EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1979/04/04 Approved Prior to Jan 1, 1982 LILLY Discontinued
CECLOR 050522 001 NDA CEFACLOR FOR SUSPENSION;ORAL EQ 125MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1979/04/04 Approved Prior to Jan 1, 1982 LILLY Discontinued
CECLOR 050522 002 NDA CEFACLOR FOR SUSPENSION;ORAL EQ 250MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1979/04/04 Approved Prior to Jan 1, 1982 LILLY Discontinued
CECLOR CD 050673 001 NDA CEFACLOR TABLET, EXTENDED RELEASE;ORAL EQ 375MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1996/06/28 1996/06/28 LILLY Discontinued
CECLOR CD 050673 002 NDA CEFACLOR TABLET, EXTENDED RELEASE;ORAL EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1996/06/28 1996/06/28 LILLY Discontinued
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