美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=LODINE"
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
TRIALODINE 070942 001 ANDA TRAZODONE HYDROCHLORIDE TABLET;ORAL 50MG No No -- 1986/12/01 QUANTUM PHARMICS Discontinued
LODINE 018922 002 NDA ETODOLAC CAPSULE;ORAL 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1991/01/31 1991/01/31 WYETH PHARMS INC Discontinued
LODINE 018922 003 NDA ETODOLAC CAPSULE;ORAL 300MG Yes No 1991/01/31 1991/01/31 WYETH PHARMS INC Discontinued
LODINE 018922 004 NDA ETODOLAC TABLET;ORAL 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1991/01/31 1993/07/29 WYETH PHARMS INC Discontinued
LODINE 018922 005 NDA ETODOLAC TABLET;ORAL 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1991/01/31 1996/06/28 WYETH PHARMS INC Discontinued
LODINE XL 020584 001 NDA ETODOLAC TABLET, EXTENDED RELEASE;ORAL 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1996/10/25 1996/10/25 WYETH PHARMS INC Discontinued
LODINE XL 020584 002 NDA ETODOLAC TABLET, EXTENDED RELEASE;ORAL 600MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1996/10/25 1996/10/25 WYETH PHARMS INC Discontinued
LODINE XL 020584 003 NDA ETODOLAC TABLET, EXTENDED RELEASE;ORAL 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1996/10/25 1998/01/20 WYETH PHARMS INC Discontinued
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