Visitor Monitoring Drug History: BETOPTIC
 
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: BETOPTIC
FDA Application No: (NDA) 019270
Active Ingredient(s): BETAXOLOL HYDROCHLORIDE
Company: ALCON
 
Label History
 
View the label approved on February 22, 2006 for BETOPTIC, (NDA) 019270


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
2/14/2006 031Labeling Revision Letter
Label 
12/4/2002 029Control Supplement  
3/13/2002 028Control Supplement  
3/16/2001 027Control Supplement  
2/18/2000 026Manufacturing Change or Addition  
8/17/1999 025Control Supplement  
4/7/1999 024Manufacturing Change or Addition  
3/26/1999 023Package Change  
2/5/1999 022Manufacturing Change or Addition  
3/11/1999 021Control Supplement  
8/4/1998 020Control Supplement  
1/15/1998 019Manufacturing Change or Addition  
11/1/1995 018Control Supplement  
11/1/1995 017Control Supplement  
1/22/1993 016Manufacturing Change or Addition  
4/10/1991 015Package Change  
2/14/1991 014Control Supplement  
7/9/1990 013Package Change  
7/19/1989 012Manufacturing Change or Addition  
10/28/1991 011Labeling Revision  
8/31/1988 010Manufacturing Change or Addition  
7/13/1988 009Manufacturing Change or Addition  
9/24/1987 008Control Supplement  
7/7/1986 007Package Change  
11/4/1986 006Manufacturing Change or Addition  
5/27/1986 004Control Supplement  
12/12/1985 002Package Change  
12/12/1985 001Manufacturing Change or Addition  
8/30/1985 000Approval  
 
Therapeutic Equivalents
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