PAROXETINE HYDROCHLORIDE Detail

Drug Name(s):
PAROXETINE HYDROCHLORIDE

FDA Application No.:
NDA 075566

Active Ingredient(s):
PAROXETINE HYDROCHLORIDE

Company:
SANDOZ

Original Approval or Tentative Approval Date:
March 7, 2004

Products on Application NDA 075566:

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

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January 2009

PAROXETINE HYDROCHLORIDE Detail

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