美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=LOXITANE"
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
LOXITANE 017525 001 NDA LOXAPINE SUCCINATE CAPSULE;ORAL EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1975/02/25 Approved Prior to Jan 1, 1982 ACTAVIS LABS UT INC Discontinued
LOXITANE 017525 002 NDA LOXAPINE SUCCINATE CAPSULE;ORAL EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1975/02/25 Approved Prior to Jan 1, 1982 ACTAVIS LABS UT INC Discontinued
LOXITANE 017525 003 NDA LOXAPINE SUCCINATE CAPSULE;ORAL EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1975/02/25 Approved Prior to Jan 1, 1982 ACTAVIS LABS UT INC Discontinued
LOXITANE 017525 004 NDA LOXAPINE SUCCINATE CAPSULE;ORAL EQ 50MG BASE *Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1975/02/25 Approved Prior to Jan 1, 1982 ACTAVIS LABS UT INC Discontinued
LOXITANE 017525 006 NDA LOXAPINE SUCCINATE TABLET;ORAL EQ 10MG BASE **Federal Register determination that product was discontinued or withdrawn for s or e reasons** Yes No 1975/02/25 Approved Prior to Jan 1, 1982 ACTAVIS LABS UT INC Discontinued
LOXITANE 017525 007 NDA LOXAPINE SUCCINATE TABLET;ORAL EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1975/02/25 Approved Prior to Jan 1, 1982 ACTAVIS LABS UT INC Discontinued
LOXITANE 017525 008 NDA LOXAPINE SUCCINATE TABLET;ORAL EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1975/02/25 Approved Prior to Jan 1, 1982 ACTAVIS LABS UT INC Discontinued
LOXITANE C 017658 001 NDA LOXAPINE HYDROCHLORIDE CONCENTRATE;ORAL EQ 25MG BASE/ML No No 1976/05/04 Approved Prior to Jan 1, 1982 ACTAVIS LABS UT INC Discontinued
LOXITANE IM 018039 001 NDA LOXAPINE HYDROCHLORIDE INJECTABLE;INJECTION EQ 50MG BASE/ML No No 1979/10/26 Approved Prior to Jan 1, 1982 ACTAVIS LABS UT INC Discontinued
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