DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
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 Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/4/2002
007
Manufacturing Change or Addition
11/30/1998
006
Manufacturing Change or Addition
9/24/1997
005
Control Supplement
6/15/1995
004
Package Change
1/30/1990
003
Control Supplement
7/5/1990
002
New Dosage Regimen
4/5/1989
001
New or Modified Indication
2/29/1988
000
Approval
There are no Therapeutic Equivalents
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