Visitor Monitoring Drug History: WYTENSIN
 
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: WYTENSIN
FDA Application No: (NDA) 018587
Active Ingredient(s): GUANABENZ ACETATE
Company: WYETH AYERST
 
Label History
 
Labels are not available on this site for WYTENSIN, (NDA) 018587
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/27/2001 023Labeling Revision  
7/23/1997 022Labeling Revision  
7/31/1991 021Labeling Revision  
1/25/1989 020Labeling Revision  
9/22/1988 019Labeling Revision  
4/8/1988 018Package Change  
4/11/1989 017Package Change  
10/22/1986 015Labeling Revision  
3/26/1986 014Manufacturing Change or Addition  
2/4/1986 013Formulation Revision  
4/18/1986 012Control Supplement  
4/29/1987 011Labeling Revision  
12/18/1985 010Control Supplement  
10/18/1985 009Labeling Revision  
9/26/1984 006Control Supplement  
6/26/1984 005Labeling Revision  
2/27/1984 004Labeling Revision  
12/23/1983 003Package Change  
6/21/1983 002Control Supplement  
6/20/1983 001Control Supplement  
9/7/1982 000Approval  
 
Therapeutic Equivalents
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