Visitor Monitoring Drug History: FENOFIBRATE
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: FENOFIBRATE
FDA Application No: (NDA) 022118
Active Ingredient(s): FENOFIBRATE
Company: LIFECYCLE PHARMA AS
 
Label History
 
View the label approved on August 14, 2007 for FENOFIBRATE, (NDA) 022118


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/10/2007 000Approval Letter
Label 
 
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