DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
TAVIST
FDA Application No:
(NDA) 018675
Active Ingredient(s):
CLEMASTINE FUMARATE
Company:
NOVARTIS
Label History
Labels are not available on this site for TAVIST, (NDA) 018675
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/11/2002
010
Manufacturing Change or Addition
6/14/1995
007
Control Supplement
8/30/1994
006
Labeling Revision
7/21/1994
004
Control Supplement
12/4/1987
002
Control Supplement
12/2/1986
001
Control Supplement
6/28/1985
000
Approval
There are no Therapeutic Equivalents
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