Visitor Monitoring Drug Details: ABILIFY
 
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Drug Details

Drug Name: ABILIFY
FDA Application No: (NDA) 021729
Active Ingredient(s): ARIPIPRAZOLE
Company: OTSUKA
Original Approval or Tentative Approval Date: June 7, 2006
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Label Information
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
ABILIFY ARIPIPRAZOLE10MGTABLET, ORALLY DISINTEGRATING; ORAL Prescription Yes None
ABILIFY ARIPIPRAZOLE15MGTABLET, ORALLY DISINTEGRATING; ORAL Prescription No None
ABILIFY ARIPIPRAZOLE20MGTABLET, ORALLY DISINTEGRATING; ORAL Prescription No None
ABILIFY ARIPIPRAZOLE30MGTABLET, ORALLY DISINTEGRATING; ORAL Prescription No None


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