Visitor Monitoring Drug History: KEPPRA
 
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: KEPPRA
FDA Application No: (NDA) 021505
Active Ingredient(s): LEVETIRACETAM
Company: UCB INC
 
Label History
 
View the label approved on March 23, 2007 for KEPPRA, (NDA) 021505


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
9/12/2007 015Labeling Revision Letter 
3/19/2007 013New or Modified Indication Letter
Label 
8/15/2006 009New or Modified Indication Letter
Label 
6/21/2005 007Patient Population Altered Letter
Label 
1/24/2006 006Labeling Revision Letter 
10/26/2004 003Labeling Revision Letter 
10/26/2004 002Labeling Revision Letter 
7/15/2003 000Approval Letter
Review
Patient Information Sheet 
 
There are no Therapeutic Equivalents
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