Visitor Monitoring Drug History: ABILIFY
 
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: ABILIFY
FDA Application No: (NDA) 021436
Active Ingredient(s): ARIPIPRAZOLE
Company: OTSUKA
 
Label History
 
View the label approved on September 26, 2007 for ABILIFY, (NDA) 021436


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
9/25/2007 016Labeling Revision Letter
Label 
9/18/2006 014Labeling Revision Letter
Label 
10/20/2006 013Labeling Revision Letter
Label 
2/16/2006 010Labeling Revision Letter
Label 
3/1/2005 008Labeling Revision Letter
Label 
6/21/2005 007Labeling Revision Letter
Label 
4/8/2004 006Labeling Revision Letter
Label 
3/1/2005 005New or Modified Indication Letter
Label 
12/30/2003 004Supplement Review 
9/29/2004 002New or Modified Indication Letter
Label 
8/28/2003 001New or Modified Indication Letter
Label
Review 
11/15/2002 000Approval Letter
Label
Review
Patient Information Sheet 
 
There are no Therapeutic Equivalents
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