Visitor Monitoring Drug History: SECTRAL
 
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: SECTRAL
FDA Application No: (NDA) 018917
Active Ingredient(s): ACEBUTOLOL HYDROCHLORIDE
Company: DR REDDYS LABS INC
 
Label History
 
View the label approved on September 11, 2007 for SECTRAL, (NDA) 018917


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
9/6/2007 024Labeling Revision Letter
Label 
7/13/2001 021Manufacturing Change or Addition  
8/22/1999 020Labeling Revision  
11/7/1997 019Labeling Revision  
8/10/1989 017Labeling Revision  
10/3/1988 016Formulation Revision  
12/5/1988 015Labeling Revision  
3/24/1989 014Manufacturing Change or Addition  
12/18/1987 013Package Change  
8/18/1987 012Package Change  
11/20/1987 011Manufacturing Change or Addition  
12/5/1988 010Package Change  
5/4/1987 008Labeling Revision  
6/11/1987 007Labeling Revision  
6/25/1986 006Labeling Revision  
6/9/1986 004Control Supplement  
8/28/1985 002Package Change  
2/6/1985 001Labeling Revision  
12/28/1984 000Approval  
 
Therapeutic Equivalents
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