美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=TRICOR"
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
TRICOR (MICRONIZED) 019304 002 NDA FENOFIBRATE CAPSULE;ORAL 67MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1993/12/31 1998/02/09 ABBVIE Discontinued
TRICOR (MICRONIZED) 019304 003 NDA FENOFIBRATE CAPSULE;ORAL 134MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1993/12/31 1999/06/30 ABBVIE Discontinued
TRICOR (MICRONIZED) 019304 004 NDA FENOFIBRATE CAPSULE;ORAL 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1993/12/31 1999/06/30 ABBVIE Discontinued
TRICOR 021203 001 NDA FENOFIBRATE TABLET;ORAL 54MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 2001/09/04 2001/09/04 ABBVIE Discontinued
TRICOR 021203 003 NDA FENOFIBRATE TABLET;ORAL 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 2001/09/04 2001/09/04 ABBVIE Discontinued
TRICOR 021656 001 NDA FENOFIBRATE TABLET;ORAL 48MG Yes No 2004/11/05 2004/11/05 ABBVIE Prescription
TRICOR 021656 002 NDA FENOFIBRATE TABLET;ORAL 145MG Yes No 2004/11/05 2004/11/05 ABBVIE Discontinued
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