DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HALOPERIDOL
FDA Application No:
(ANDA) 071211
Active Ingredient(s):
HALOPERIDOL
Company:
SANDOZ
Label History
Labels are not available on this site for HALOPERIDOL, (ANDA) 071211
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/5/2002
015
Labeling
4/19/2002
014
Control Supplement
5/9/2001
013
Control Supplement
6/14/2001
012
Control Supplement
6/28/2001
011
Control Supplement
10/16/2001
010
Labeling
10/31/2000
009
Control Supplement
4/4/2000
008
Control Supplement
5/5/1999
007
Chemistry
1/6/2000
006
Chemistry
2/2/1995
005
Chemistry
4/20/1990
004
Labeling in Effect
6/1/1989
003
Labeling
9/9/1988
002
Labeling
4/26/1988
001
Chemistry
3/11/1988
000
Approval
Therapeutic Equivalents
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