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) 019599
Active Ingredient(s): NAFTIFINE HYDROCHLORIDE
Company: MERZ PHARMS
 
Label History
 
Labels are not available on this site for NAFTIN, (NDA) 019599
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/4/2002 007Manufacturing Change or Addition  
11/30/1998 006Manufacturing Change or Addition  
9/24/1997 005Control Supplement  
6/15/1995 004Package Change  
1/30/1990 003Control Supplement  
7/5/1990 002New Dosage Regimen  
4/5/1989 001New or Modified Indication  
2/29/1988 000Approval  
 
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