Visitor Monitoring Drug History: EXNA
 
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: EXNA
FDA Application No: (NDA) 012489
Active Ingredient(s): BENZTHIAZIDE
Company: AH ROBINS INC
 
Label History
 
Labels are not available on this site for EXNA, (NDA) 012489
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/1/1994 022Labeling Revision  
9/13/1983 021Control Supplement  
12/10/1982 020Control Supplement  
7/15/1982 019Practioner Draft Labeling  
4/11/1986 018Practioner Draft Labeling  
4/12/1982 017Package Change  
2/17/1981 016Manufacturing Change or Addition  
2/13/1981 015Labeling Revision  
1/27/1981 014Control Supplement  
4/18/1979 013Control Supplement  
4/18/1979 012Control Supplement  
4/18/1979 011Control Supplement  
4/27/1978 010Control Supplement  
4/27/1978 009Control Supplement  
4/8/1977 008Control Supplement  
6/2/1976 007Expiration Date Change  
4/2/1976 006Formulation Revision  
3/25/1975 004Labeling Revision  
10/14/1960 000Approval  
 
Therapeutic Equivalents
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