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) 021713
Active Ingredient(s): ARIPIPRAZOLE
Company: OTSUKA PHARM
 
Label History
 
View the label approved on September 26, 2007 for ABILIFY, (NDA) 021713


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 010Labeling Revision Letter
Label 
9/18/2006 009Labeling Revision Letter
Label 
10/20/2006 008Labeling Revision Letter
Label 
2/16/2006 006Labeling Revision Letter
Label 
6/21/2005 004Labeling Revision Letter
Label 
3/1/2005 003Labeling Revision Letter
Label 
12/10/2004 000Approval Letter
Label
Review
Patient Information Sheet 
 
There are no Therapeutic Equivalents
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