Visitor Monitoring Drug Details: LAMIVUDINE
 
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Drug Details

Drug Name: LAMIVUDINE
FDA Application No: (NDA) 021939
Active Ingredient(s): LAMIVUDINE; ZIDOVUDINE; NEVIRAPINE
Company: AUROBINDO PHARMA LTD
Original Approval or Tentative Approval Date: January 29, 2007
 
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
LAMIVUDINE LAMIVUDINE; ZIDOVUDINE; NEVIRAPINE150MG; 300MG; 200MGTABLET; ORAL Tentative Approval No None


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