Drug Details: SEREVENT

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	SEREVENT
FDA Application No:	(NDA) 020236
Active Ingredient(s):	SALMETEROL XINAFOATE
Company:	GLAXOSMITHKLINE
Original Approval or Tentative Approval Date:	February 4, 1994
Chemical Type:	1 New molecular entity (NME)
Review Classification:	P Priority review drug

There are no Therapeutic Equivalents	Label Information
Approval History, Letters, Reviews and Related Documents

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Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code
SEREVENT	SALMETEROL XINAFOATE	EQ 0.021MG BASE/INH	AEROSOL, METERED; INHALATION	Discontinued	No	None

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