Drug Details: HALOPERIDOL LACTATE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	HALOPERIDOL LACTATE
FDA Application No:	(ANDA) 074536
Active Ingredient(s):	HALOPERIDOL LACTATE
Company:	ACTAVIS MID ATLANTIC
Original Approval or Tentative Approval Date:	November 2, 1995

There are no Therapeutic Equivalents	Labels are not available
Approval History, Letters, Reviews and Related Documents

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Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code
HALOPERIDOL LACTATE	HALOPERIDOL LACTATE	EQ 1MG BASE/ML	SOLUTION; ORAL	Prescription	No	None

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