美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=LAMIVUDINE; ZIDOVUDINE"
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
LAMIVUDINE; ZIDOVUDINE 021943 001 NDA LAMIVUDINE; ZIDOVUDINE; EFAVIRENZ TABLET; ORAL 150MG; 300MG; 600MG No No 2006/03/06 (TA) -- AUROBINDO PHARMA LTD None (Tentative Approval)
LAMIVUDINE; ZIDOVUDINE; ABACAVIR 021944 001 NDA LAMIVUDINE; ZIDOVUDINE; ABACAVIR TABLET; ORAL 150MG; 300MG; 300MG No No 2006/07/26 (TA) -- AUROBINDO PHARMA LTD None (Tentative Approval)
LAMIVUDINE; ZIDOVUDINE; NEVIRAPINE 021971 001 NDA LAMIVUDINE; ZIDOVUDINE; NEVIRAPINE TABLET; ORAL 150MG; 300MG; 200MG No No 2007/01/31 (TA) -- CIPLA LIMITED None (Tentative Approval)
LAMIVUDINE; ZIDOVUDINE; EFAVIRENZ 022096 001 NDA LAMIVUDINE; ZIDOVUDINE; EFAVIRENZ TABLET; ORAL 150MG; 300MG; 600MG No No 2007/06/01 (TA) -- STRIDES ACROLAB None (Tentative Approval)
LAMIVUDINE; ZIDOVUDINE 078929 001 ANDA LAMIVUDINE; ZIDOVUDINE TABLET; ORAL 150MG; 300MG No No 2007/08/08 (TA) -- EMCURE PHARMA None (Tentative Approval)
LAMIVUDINE; ZIDOVUDINE 022296 001 NDA LAMIVUDINE; ZIDOVUDINE TABLET; ORAL 30MG; 60MG No No 2009/07/23 (TA) -- AUROBINDO PHARMA LTD None (Tentative Approval)
LAMIVUDINE; ZIDOVUDINE 200748 001 NDA LAMIVUDINE; ZIDOVUDINE TABLET; ORAL 30MG; 60MG No No 2011/01/05 (TA) -- MATRIX LABS LTD None (Tentative Approval)
LAMIVUDINE; ZIDOVUDINE 201151 001 NDA LAMIVUDINE; ZIDOVUDINE TABLET; ORAL 30MG; 60MG No No 2011/09/22 (TA) -- CIPLA LIMITED None (Tentative Approval)
LAMIVUDINE; ZIDOVUDINE 202814 001 NDA LAMIVUDINE; ZIDOVUDINE TABLET, FOR SUSPENSION; ORAL 30MG; 60MG No No 2012/06/15 (TA) -- CIPLA LIMITED None (Tentative Approval)
LAMIVUDINE; ZIDOVUDINE 204914 001 NDA LAMIVUDINE; ZIDOVUDINE TABLET; ORAL SUSPENSION 30MG; 60MG No No 2014/02/04 (TA) -- MYLAN LABS None (Tentative Approval)
LAMIVUDINE; ZIDOVUDINE; EFAVIRENZ 206040 001 NDA LAMIVUDINE;ZIDOVUDINE;EFAVIRENZ TABLET;ORAL 150MG;300MG;600MG No No 2014/09/04 (TA) -- MYLAN LABS LTD None (Tentative Approval)
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