DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HIBICLENS
FDA Application No:
(NDA) 018423
Active Ingredient(s):
CHLORHEXIDINE GLUCONATE
Company:
REGENT
Label History
Labels are not available on this site for HIBICLENS, (NDA) 018423
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/12/2001
016
Manufacturing Change or Addition
10/19/1999
014
Package Change
7/23/1992
013
Control Supplement
7/14/1989
012
Formulation Revision
9/15/1989
011
Control Supplement
8/25/1989
010
Labeling Revision
7/5/1988
008
Manufacturing Change or Addition
6/22/1988
007
Labeling Revision
12/10/1987
006
Manufacturing Change or Addition
9/2/1988
005
Control Supplement
2/22/1986
003
Control Supplement
11/18/1983
002
Control Supplement
10/19/1981
001
Control Supplement
8/27/1981
000
Approval
Therapeutic Equivalents
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