Visitor Monitoring Drug History: NAFTIN
 
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: NAFTIN
FDA Application No: (NDA) 019356
Active Ingredient(s): NAFTIFINE HYDROCHLORIDE
Company: MERZ PHARMS
 
Label History
 
Labels are not available on this site for NAFTIN, (NDA) 019356
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/26/2007 007Package Change Letter 
7/1/2002 004Manufacturing Change or Addition  
11/30/1998 003Manufacturing Change or Addition  
9/24/1997 002Control Supplement  
7/30/1990 001Manufacturing Change or Addition  
6/18/1990 000Approval  
 
There are no Therapeutic Equivalents
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