Drug Details: ONDANSETRON HYDROCHLORIDE AND SODIUM CHLORIDE IN PLASTIC CONTAINER

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	ONDANSETRON HYDROCHLORIDE AND SODIUM CHLORIDE IN PLASTIC CONTAINER
FDA Application No:	(NDA) 021915
Active Ingredient(s):	ONDANSETRON HYDROCHLORIDE
Company:	BAXTER HLTHCARE
Original Approval or Tentative Approval Date:	December 27, 2006
Chemical Type:	3 New dosage form
Review Classification:	S Standard review drug

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
ONDANSETRON HYDROCHLORIDE AND SODIUM CHLORIDE IN PLASTIC CONTAINER	ONDANSETRON HYDROCHLORIDE	EQ 0.64MG BASE/ML	INJECTABLE; INJECTION	Prescription	Yes	AP

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