ZOLOFT Detail

Drug Name(s):
ZOLOFT

FDA Application No.:
NDA 019839

Active Ingredient(s):
SERTRALINE HYDROCHLORIDE

Company:
PFIZER

Original Approval or Tentative Approval Date:
December 29, 1991

Products on Application NDA 019839:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
SERTRALINE HYDROCHLORIDE	EQ 100MG BASE	TABLET; ORAL	Prescription	AB
SERTRALINE HYDROCHLORIDE	EQ 200MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET; ORAL	Discontinued	none

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last updated on 11-21-2008

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