Visitor Monitoring Drug History: NATURETIN-5
 
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: NATURETIN-5
FDA Application No: (NDA) 012164
Active Ingredient(s): BENDROFLUMETHIAZIDE
Company: APOTHECON
 
Label History
 
Labels are not available on this site for NATURETIN5, (NDA) 012164
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/2/1997 028Manufacturing Change or Addition  
10/1/1996 027Control Supplement  
8/7/1991 026Manufacturing Change or Addition  
3/11/1993 025Manufacturing Change or Addition  
6/4/1982 023Formulation Revision  
2/19/1982 022Manufacturing Change or Addition  
12/15/1981 021Formulation Revision  
6/16/1989 020Practioner Draft Labeling  
5/4/1979 019Labeling Revision  
6/16/1977 018Labeling Revision  
6/16/1977 017Control Supplement  
12/29/1976 016Labeling Revision  
12/7/1959 000Approval  
 
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