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) 071212
Active Ingredient(s):
HALOPERIDOL
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for HALOPERIDOL, (ANDA) 071212
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/1/1998
015
Chemistry
12/23/1994
014
Chemistry
10/11/1994
013
Chemistry
4/3/1992
012
Chemistry
4/3/1992
011
Chemistry
1/19/1995
009
Chemistry
10/27/1989
008
SBA
9/12/1990
007
Chemistry
9/12/1990
005
Labeling
9/12/1990
004
Chemistry
1/19/1995
003
Chemistry
3/15/1988
001
Chemistry
1/7/1988
000
Approval
Therapeutic Equivalents
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