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) 071207
Active Ingredient(s):
HALOPERIDOL
Company:
SANDOZ
Label History
Labels are not available on this site for HALOPERIDOL, (ANDA) 071207
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/5/2002
020
Labeling
5/9/2001
019
Control Supplement
6/28/2001
018
Control Supplement
10/16/2001
017
Labeling
10/31/2000
016
Control Supplement
4/4/2000
015
Control Supplement
5/5/1999
014
Chemistry
1/6/2000
013
Chemistry
9/18/1998
012
Labeling
9/21/1998
011
Chemistry
2/2/1995
010
Chemistry
3/29/1990
009
SBA
4/20/1990
009
Labeling in Effect
4/4/1991
008
Chemistry
6/1/1989
007
Labeling
9/9/1988
006
Labeling
10/28/1987
003
Chemistry
10/28/1987
002
Chemistry
11/17/1986
000
Approval
Therapeutic Equivalents
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