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) 073037
Active Ingredient(s):
HALOPERIDOL LACTATE
Company:
PHARM ASSOC
Label History
Labels are not available on this site for HALOPERIDOL, (ANDA) 073037
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/27/1995
004
Chemistry
1/31/1995
003
Labeling
1/31/1995
002
Chemistry
2/26/1993
000
Approval
Therapeutic Equivalents
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