Drug Details: HALDOL

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	HALDOL
FDA Application No:	(NDA) 015922
Active Ingredient(s):	HALOPERIDOL LACTATE
Company:	ORTHO MCNEIL
Original Approval or Tentative Approval Date:	April 12, 1967
Chemical Type:	3 New dosage form
Review Classification:	P Priority review drug

Therapeutic Equivalents	Labels are not available
Approval History, Letters, Reviews and Related Documents

You can see the products in the same application. The table can be sorted by clicking the header columns.

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code
HALDOL	HALOPERIDOL LACTATE	EQ 2MG BASE/ML	CONCENTRATE; ORAL	Discontinued	No	None

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