Visitor Monitoring Drug History: RESERPINE
 
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: RESERPINE
FDA Application No: (NDA) 009838
Active Ingredient(s): RESERPINE
Company: SANDOZ
 
Label History
 
Labels are not available on this site for RESERPINE, (NDA) 009838
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/8/1999 035Manufacturing Change or Addition  
9/7/1999 034Control Supplement  
11/6/1996 033Labeling Revision  
3/15/1996 032Control Supplement  
 
Therapeutic Equivalents
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