Visitor Monitoring Drug History: ALAWAY
 
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: ALAWAY
FDA Application No: (NDA) 021996
Active Ingredient(s): KETOTIFEN FUMARATE
Company: BAUSCH AND LOMB
 
Label History
 
View the label approved on April 20, 2007 for ALAWAY, (NDA) 021996


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
4/18/2007 001Package Change Letter
Label 
12/1/2006 000Approval Letter 
 
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