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Drug Details
Drug Name(s) SELZENTRY (Brand Name Drug)
FDA Application No. (NDA) 022128
Active Ingredient(s) MARAVIROC
Company PFIZER
Original Approval or Tentative Approval Date August 6, 2007
Chemical Type 1  New molecular entity (NME)
Review Classification P  Priority review drug  

  • There are no Therapeutic Equivalents

Products on Application (NDA) #022128
    Click on a column header to re-sort the table:

Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing
Status
RLD
TE
Code
SELZENTRY  MARAVIROC  150MG  TABLET; ORAL  Prescription  No None  
SELZENTRY  MARAVIROC  300MG  TABLET; ORAL  Prescription  Yes None  

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