Visitor Monitoring Drug History: KERLONE
 
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: KERLONE
FDA Application No: (NDA) 019507
Active Ingredient(s): BETAXOLOL HYDROCHLORIDE
Company: SANOFI AVENTIS US
 
Label History
 
Labels are not available on this site for KERLONE, (NDA) 019507
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/27/1995 005Package Change  
6/1/1992 004Labeling Revision  
10/26/1990 002Control Supplement  
7/5/1990 001Labeling Revision  
10/27/1989 000Approval  
 
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