Visitor Monitoring Drug Details: FENOFIBRATE (MICRONIZED)
 
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Drug Details

Drug Name: FENOFIBRATE (MICRONIZED)
FDA Application No: (ANDA) 075753
Active Ingredient(s): FENOFIBRATE
Company: TEVA
Original Approval or Tentative Approval Date: April 9, 2002
 
 
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
FENOFIBRATE (MICRONIZED) FENOFIBRATE67MGCAPSULE; ORAL Prescription No AB
FENOFIBRATE (MICRONIZED) FENOFIBRATE134MGCAPSULE; ORAL Prescription No AB
FENOFIBRATE (MICRONIZED) FENOFIBRATE200MGCAPSULE; ORAL Prescription Yes AB


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