Visitor Monitoring Drug History: BETOPTIC S
 
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 S
FDA Application No: (NDA) 019845
Active Ingredient(s): BETAXOLOL HYDROCHLORIDE
Company: ALCON
 
Label History
 
View the label approved on June 12, 2007 for BETOPTIC S, (NDA) 019845


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
6/8/2007 020Patient Population Altered Letter
Label 
5/9/2003 017Labeling Revision Letter
Label 
12/4/2002 016Control Supplement  
3/16/2001 015Control Supplement  
2/18/2000 014Manufacturing Change or Addition  
8/17/1999 013Control Supplement  
4/7/1999 012Manufacturing Change or Addition  
4/5/1999 011Manufacturing Change or Addition  
2/5/1999 010Manufacturing Change or Addition  
3/11/1999 009Control Supplement  
10/14/1998 008Control Supplement  
2/23/1999 007Manufacturing Change or Addition  
8/27/1998 006Control Supplement  
11/1/1995 005Control Supplement  
11/1/1995 004Control Supplement  
1/22/1993 003Manufacturing Change or Addition  
4/10/1991 002Package Change  
12/20/1990 001Labeling Revision  
12/29/1989 000Approval  
 
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