Visitor Monitoring Drug History: ENDURON
 
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: ENDURON
FDA Application No: (NDA) 012524
Active Ingredient(s): METHYCLOTHIAZIDE
Company: ABBOTT
 
Label History
 
Labels are not available on this site for ENDURON, (NDA) 012524
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/16/1998 034Package Change  
8/29/1986 032Control Supplement  
1/25/1984 031Control Supplement  
6/23/1982 030Labeling Revision  
7/26/1988 029Practioner Draft Labeling  
6/15/1981 027Labeling Revision  
6/15/1981 026Labeling Revision  
10/21/1960 000Approval  
 
Therapeutic Equivalents
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