Visitor Monitoring Drug History: BETAGAN
 
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: BETAGAN
FDA Application No: (NDA) 019219
Active Ingredient(s): LEVOBUNOLOL HYDROCHLORIDE
Company: ALLERGAN
 
Label History
 
View the label approved on April 15, 2003 for BETAGAN, (NDA) 019219


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
4/12/2002 023Manufacturing Change or Addition  
12/4/2001 022Manufacturing Change or Addition  
4/12/2001 021Manufacturing Change or Addition  
8/8/2001 020Manufacturing Change or Addition Label 
5/14/2001 019Labeling Revision  
10/2/2000 018Manufacturing Change or Addition  
5/19/1998 017Control Supplement  
5/1/1998 016Control Supplement  
2/12/1998 015Manufacturing Change or Addition  
6/12/1995 014Manufacturing Change or Addition  
8/3/1995 013Control Supplement  
1/13/1994 012Control Supplement  
2/3/1992 011Labeling Revision  
1/31/1990 010Labeling Revision  
12/6/1989 009Package Change  
12/4/1989 007Labeling Revision  
11/9/1988 005Labeling Revision  
10/21/1988 004Control Supplement  
8/13/1987 003Labeling Revision  
9/15/1987 002Control Supplement  
12/19/1985 000Approval  
 
Therapeutic Equivalents
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