Visitor Monitoring Drug History: TENUATE
 
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: TENUATE
FDA Application No: (NDA) 017668
Active Ingredient(s): DIETHYLPROPION HYDROCHLORIDE
Company: SANOFI AVENTIS US
 
Label History
 
Labels are not available on this site for TENUATE, (NDA) 017668
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/18/1981 010Labeling Revision  
5/27/1980 009Labeling Revision  
5/12/1980 008Formulation Revision  
11/2/1979 007Control Supplement  
4/27/1978 006Package Change  
9/24/1976 004Package Change  
9/24/1976 003Package Change  
3/10/1976 002Package Change  
3/20/1975 000Approval  
 
Therapeutic Equivalents
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