Drug Details: ZOLOFT

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	ZOLOFT
FDA Application No:	(NDA) 019839
Active Ingredient(s):	SERTRALINE HYDROCHLORIDE
Company:	PFIZER
Original Approval or Tentative Approval Date:	December 30, 1991
Chemical Type:	1 New molecular entity (NME)
Review Classification:	S Standard review drug

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
ZOLOFT	SERTRALINE HYDROCHLORIDE	EQ 50MG BASE	TABLET; ORAL	Prescription	No	AB
ZOLOFT	SERTRALINE HYDROCHLORIDE	EQ 100MG BASE	TABLET; ORAL	Prescription	Yes	AB
ZOLOFT	SERTRALINE HYDROCHLORIDE	EQ 150MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET; ORAL	Discontinued	No	None
ZOLOFT	SERTRALINE HYDROCHLORIDE	EQ 200MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET; ORAL	Discontinued	No	None
ZOLOFT	SERTRALINE HYDROCHLORIDE	EQ 25MG BASE	TABLET; ORAL	Prescription	No	AB

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