Visitor Monitoring Drug History: MAZANOR
 
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: MAZANOR
FDA Application No: (NDA) 017980
Active Ingredient(s): MAZINDOL
Company: WYETH AYERST
 
Label History
 
Labels are not available on this site for MAZANOR, (NDA) 017980
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/6/1995 012Formulation Revision  
10/6/1995 011Manufacturing Change or Addition  
6/27/1991 010Manufacturing Change or Addition  
2/16/1990 009Manufacturing Change or Addition  
6/8/1987 007Package Change  
12/13/1985 005Labeling Revision  
9/15/1982 004Control Supplement  
2/2/1982 003Labeling Revision  
9/8/1981 002Package Change  
2/11/1981 001Formulation Revision  
8/28/1980 000Approval  
 
Therapeutic Equivalents
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