Drug Details: TAVIST

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	TAVIST
FDA Application No:	(NDA) 018675
Active Ingredient(s):	CLEMASTINE FUMARATE
Company:	NOVARTIS
Original Approval or Tentative Approval Date:	June 28, 1985
Chemical Type:	3 New dosage form
Review Classification:	S Standard review drug

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
TAVIST	CLEMASTINE FUMARATE	EQ 0.5MG BASE/5ML Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	SYRUP; ORAL	Discontinued	No	None

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