Visitor Monitoring Drug Details: REFLUDAN
 
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Drug Details

Drug Name: REFLUDAN
FDA Application No: (NDA) 020807
Active Ingredient(s): LEPIRUDIN RECOMBINANT
Company: BAYER HLTHC
Original Approval or Tentative Approval Date: March 6, 1998
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
O Orphan drug
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
REFLUDAN LEPIRUDIN RECOMBINANT50MG/VIALINJECTABLE; INJECTION Prescription Yes None


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