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) 071234
Active Ingredient(s):
HALOPERIDOL
Company:
PAR PHARM
Label History
Labels are not available on this site for HALOPERIDOL, (ANDA) 071234
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/30/1998
014
Chemistry
10/27/1993
013
Labeling
3/9/1989
012
Labeling
11/20/1987
004
Chemistry
9/15/1987
003
Chemistry
7/2/1987
001
Chemistry
11/3/1986
000
Approval
Therapeutic Equivalents
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