Visitor Monitoring Drug Details: INTEGRILIN
 
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Drug Details

Drug Name: INTEGRILIN
FDA Application No: (NDA) 020718
Active Ingredient(s): EPTIFIBATIDE
Company: SCHERING
Original Approval or Tentative Approval Date: May 18, 1998
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
 
 
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
INTEGRILIN EPTIFIBATIDE2MG/MLINJECTABLE; INJECTION Prescription Yes None
INTEGRILIN EPTIFIBATIDE75MG/100MLINJECTABLE; INJECTION Prescription Yes None


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