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) 070981
Active Ingredient(s):
HALOPERIDOL
Company:
WATSON LABS
Label History
Labels are not available on this site for HALOPERIDOL, (ANDA) 070981
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/6/1994
009
Chemistry
1/7/1991
008
Labeling
11/19/1990
007
Chemistry
5/31/1991
006
Chemistry
9/27/1988
005
SBA
6/29/1990
005
Chemistry
10/21/1988
004
Chemistry
10/21/1988
003
Chemistry
10/18/1988
001
Chemistry
3/6/1987
000
Approval
Therapeutic Equivalents
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