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
 
Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
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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