Visitor Monitoring Drug History: ENDURONYL FORTE
 
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: ENDURONYL FORTE
FDA Application No: (NDA) 012775
Active Ingredient(s): DESERPIDINE; METHYCLOTHIAZIDE
Company: ABBOTT
 
Label History
 
Labels are not available on this site for ENDURONYL FORTE, (NDA) 012775
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/16/1998 036Package Change  
9/25/1991 035Labeling Revision  
11/17/1987 034Expiration Date Change  
9/25/1991 033Labeling Revision  
8/29/1986 032Control Supplement  
7/28/1986 031Control Supplement  
1/5/1984 030Labeling Revision  
8/25/1982 029Labeling Revision  
10/5/1981 027Formulation Revision  
5/22/1981 026Control Supplement  
3/27/1981 025Control Supplement  
12/12/1980 024Formulation Revision  
1/3/1980 023Labeling Revision  
8/1/1961 000Approval  
 
There are no Therapeutic Equivalents
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