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) 071015
Active Ingredient(s):
HALOPERIDOL LACTATE
Company:
TEVA
Label History
Labels are not available on this site for HALOPERIDOL, (ANDA) 071015
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/30/2001
017
Facility Addition
7/7/2000
016
Facility Addition
7/8/1997
015
Chemistry
11/2/1994
014
Chemistry
11/2/1994
013
Chemistry
11/2/1994
012
Chemistry
10/21/1993
011
Chemistry
10/21/1993
010
Chemistry
10/21/1993
009
Chemistry
10/21/1993
008
Chemistry
10/21/1993
007
Chemistry
10/21/1993
006
Chemistry
9/8/1993
005
Chemistry
6/12/1989
004
Labeling
8/29/1989
003
Chemistry
9/22/1988
002
Labeling
1/27/1989
001
Chemistry
8/25/1987
000
Approval
Therapeutic Equivalents
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