Visitor Monitoring Drug History: BETAXON
 
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: BETAXON
FDA Application No: (NDA) 021114
Active Ingredient(s): LEVOBETAXOLOL HYDROCHLORIDE
Company: ALCON
 
Label History
 
View the label approved on February 29, 2000 for BETAXON, (NDA) 021114


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
6/11/2006 011Labeling Revision  
9/28/2006 002Efficacy Supplement with Clinical Data to Support Letter 
2/23/2000 000Approval Letter
Label
Review 
 
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