Visitor Monitoring Drug History: KETOTIFEN FUMARATE
 
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Label and Approval History

Drug Name: KETOTIFEN FUMARATE
FDA Application No: (ANDA) 077958
Active Ingredient(s): KETOTIFEN FUMARATE
Company: AKORN
 
Label History
 
Labels are not available on this site for KETOTIFEN FUMARATE, (ANDA) 077958
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/26/2007 000Approval Patient Information Sheet 
 
Therapeutic Equivalents
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