美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=UNIPEN"
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
UNIPEN 062717 001 ANDA NAFCILLIN SODIUM INJECTABLE;INJECTION EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No -- 1986/12/16 WYETH AYERST Discontinued
UNIPEN 062717 002 ANDA NAFCILLIN SODIUM INJECTABLE;INJECTION EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No -- 1986/12/16 WYETH AYERST Discontinued
UNIPEN 062717 004 ANDA NAFCILLIN SODIUM INJECTABLE;INJECTION EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No -- 1986/12/16 WYETH AYERST Discontinued
UNIPEN 050199 001 NDA NAFCILLIN SODIUM FOR SOLUTION;ORAL EQ 250MG BASE/5ML No No 1965/10/11 Approved Prior to Jan 1, 1982 WYETH AYERST Discontinued
UNIPEN 050111 001 NDA NAFCILLIN SODIUM CAPSULE;ORAL EQ 250MG BASE No No 1970/04/07 Approved Prior to Jan 1, 1982 WYETH AYERST Discontinued
UNIPEN 050320 001 NDA NAFCILLIN SODIUM INJECTABLE;INJECTION EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1970/06/23 Approved Prior to Jan 1, 1982 WYETH AYERST Discontinued
UNIPEN IN PLASTIC CONTAINER 050320 002 NDA NAFCILLIN SODIUM INJECTABLE;INJECTION EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1970/06/23 Approved Prior to Jan 1, 1982 WYETH AYERST Discontinued
UNIPEN 050320 003 NDA NAFCILLIN SODIUM INJECTABLE;INJECTION EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1970/06/23 Approved Prior to Jan 1, 1982 WYETH AYERST Discontinued
UNIPEN 050320 004 NDA NAFCILLIN SODIUM INJECTABLE;INJECTION EQ 4GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1970/06/23 Approved Prior to Jan 1, 1982 WYETH AYERST Discontinued
UNIPEN 050320 005 NDA NAFCILLIN SODIUM INJECTABLE;INJECTION EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1970/06/23 Approved Prior to Jan 1, 1982 WYETH AYERST Discontinued
UNIPEN 050320 006 NDA NAFCILLIN SODIUM INJECTABLE;INJECTION EQ 20GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1970/06/23 Approved Prior to Jan 1, 1982 WYETH AYERST Discontinued
UNIPEN 050462 001 NDA NAFCILLIN SODIUM TABLET;ORAL EQ 500MG BASE No No 1973/10/16 Approved Prior to Jan 1, 1982 WYETH AYERST Discontinued
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