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) 073364
Active Ingredient(s):
HALOPERIDOL LACTATE
Company:
SILARX
Label History
Labels are not available on this site for HALOPERIDOL, (ANDA) 073364
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/10/2002
004
Labeling
9/22/2000
003
Package Change
9/8/1998
002
Chemistry
7/27/1998
001
Chemistry
9/28/1993
000
Approval
Therapeutic Equivalents
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