PAXIL Detail

Drug Name(s):
PAXIL

FDA Application No.:
NDA 020031

Active Ingredient(s):
PAROXETINE HYDROCHLORIDE

Company:
GLAXOSMITHKLINE

Original Approval or Tentative Approval Date:
December 28, 1992

Products on Application NDA 020031:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
PAROXETINE HYDROCHLORIDE	EQ 10MG BASE	TABLET; ORAL	Prescription	AB
PAROXETINE HYDROCHLORIDE	EQ 30MG BASE	TABLET; ORAL	Prescription	AB
PAROXETINE HYDROCHLORIDE	EQ 40MG BASE	TABLET; ORAL	Prescription	AB

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last updated on 11-21-2008

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