Drug Details: PAXIL

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	PAXIL
FDA Application No:	(NDA) 020885
Active Ingredient(s):	PAROXETINE HYDROCHLORIDE
Company:	GLAXOSMITHKLINE
Original Approval or Tentative Approval Date:	October 9, 1998
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
PAXIL	PAROXETINE HYDROCHLORIDE	EQ 10MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	CAPSULE; ORAL	Discontinued	No	None
PAXIL	PAROXETINE HYDROCHLORIDE	EQ 20MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	CAPSULE; ORAL	Discontinued	No	None
PAXIL	PAROXETINE HYDROCHLORIDE	EQ 30MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	CAPSULE; ORAL	Discontinued	No	None
PAXIL	PAROXETINE HYDROCHLORIDE	EQ 40MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	CAPSULE; ORAL	Discontinued	No	None

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