DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HALOPERIDOL LACTATE
FDA Application No:
(ANDA) 074536
Active Ingredient(s):
HALOPERIDOL LACTATE
Company:
ACTAVIS MID ATLANTIC
Label History
Labels are not available on this site for HALOPERIDOL LACTATE, (ANDA) 074536
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/2/1995
000
Approval
There are no Therapeutic Equivalents
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