DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HALOPERIDOL DECANOATE
FDA Application No:
(ANDA) 074893
Active Ingredient(s):
HALOPERIDOL DECANOATE
Company:
ABRAXIS PHARM
Label History
Labels are not available on this site for HALOPERIDOL DECANOATE, (ANDA) 074893
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/5/2002
004
Facility Addition
11/19/1999
002
Control Supplement
1/21/1999
001
Chemistry
12/19/1997
000
Approval
Therapeutic Equivalents
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