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) 071617
Active Ingredient(s):
HALOPERIDOL LACTATE
Company:
TEVA PHARMS
Label History
Labels are not available on this site for HALOPERIDOL, (ANDA) 071617
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/31/2001
019
Facility Addition
10/31/2001
018
Facility Addition
10/31/2001
017
Facility Addition
10/25/2001
016
Package Change
10/25/2001
015
Manufacturing Revision
10/25/2001
014
Facility Addition
1/23/2002
013
Facility Addition
2/26/2001
012
Facility Addition
10/27/2000
011
Manufacturing Revision
6/17/1999
009
Chemistry
3/23/1999
008
Chemistry
5/13/1999
007
Chemistry
12/7/1998
006
Chemistry
6/2/1997
005
Labeling
5/31/1996
004
Chemistry
1/29/1993
003
Chemistry
10/10/1991
002
Labeling
10/21/1992
001
Chemistry
12/1/1988
000
Approval
Therapeutic Equivalents
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