NEFAZODONE HYDROCHLORIDE Detail

Drug Name(s):
NEFAZODONE HYDROCHLORIDE

FDA Application No.:
NDA 076072

Active Ingredient(s):
NEFAZODONE HYDROCHLORIDE

Company:
SANDOZ

Original Approval or Tentative Approval Date:
September 15, 2003

Products on Application NDA 076072:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NEFAZODONE HYDROCHLORIDE	100MG	TABLET; ORAL	Prescription	AB
NEFAZODONE HYDROCHLORIDE	200MG	TABLET; ORAL	Prescription	AB

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last updated on 12-05-2008