美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=SUPRAX"
符合检索条件的记录共 11 条
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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
SUPRAX 050621 001 NDA CEFIXIME TABLET;ORAL 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1989/04/28 1989/04/28 LEDERLE Discontinued
SUPRAX 050621 002 NDA CEFIXIME TABLET;ORAL 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1989/04/28 1989/04/28 LEDERLE Discontinued
SUPRAX 050622 001 NDA CEFIXIME FOR SUSPENSION;ORAL 100MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1989/04/28 1989/04/28 LEDERLE Discontinued
SUPRAX 065130 001 ANDA CEFIXIME TABLET;ORAL 400MG No No 2004/02/12 2004/02/12 LUPIN PHARMS Discontinued
SUPRAX 065129 001 ANDA CEFIXIME FOR SUSPENSION;ORAL 100MG/5ML No No 2004/02/23 2004/02/23 LUPIN PHARMS Discontinued
SUPRAX 065355 001 ANDA CEFIXIME FOR SUSPENSION;ORAL 200MG/5ML No Yes 2007/04/10 2007/04/10 LUPIN PHARMS Prescription
SUPRAX 065380 001 ANDA CEFIXIME TABLET, CHEWABLE;ORAL 100MG No No 2010/10/25 2010/10/25 LUPIN LTD Prescription
SUPRAX 065380 002 ANDA CEFIXIME TABLET, CHEWABLE;ORAL 150MG No No 2010/10/25 2010/10/25 LUPIN LTD Prescription
SUPRAX 065380 003 ANDA CEFIXIME TABLET, CHEWABLE;ORAL 200MG No Yes 2010/10/25 2010/10/25 LUPIN LTD Prescription
SUPRAX 203195 001 NDA CEFIXIME CAPSULE;ORAL 400MG Yes Yes 2012/06/01 2012/06/01 LUPIN LTD Prescription
SUPRAX 202091 001 NDA CEFIXIME FOR SUSPENSION;ORAL 500MG/5ML Yes Yes 2013/02/20 2013/02/20 LUPIN LTD Prescription
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