DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HIVID
FDA Application No:
(NDA) 020199
Active Ingredient(s):
ZALCITABINE
Company:
ROCHE
Label History
View the
label approved on September 12, 2002
for HIVID, (NDA) 020199
To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/2/2002
017
Control Supplement
9/12/2002
016
Labeling Revision
Letter
Label
8/14/2002
015
Labeling Revision
Letter
Label
7/3/2002
014
Labeling Revision
Letter
Label
6/1/1999
013
Labeling Revision
4/19/2000
012
Labeling Revision
8/28/1998
011
Labeling Revision
3/4/1998
010
Labeling Revision
10/15/1997
009
Control Supplement
10/4/1996
008
Labeling Revision
6/26/1996
007
New or Modified Indication
3/4/1996
006
Control Supplement
7/8/1994
005
Control Supplement
10/7/1994
004
Labeling Revision
8/5/1994
003
Accelerated Approval
10/7/1994
002
Labeling Revision
4/13/1994
001
Control Supplement
6/19/1992
000
Approval
There are no Therapeutic Equivalents
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