FAMVIR Detail

Drug Name(s):
FAMVIR

FDA Application No.:
NDA 020363

Active Ingredient(s):
FAMCICLOVIR

Company:
NOVARTIS

Original Approval or Tentative Approval Date:
December 26, 1994

Products on Application NDA 020363:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
FAMCICLOVIR	125MG	TABLET; ORAL	Prescription	none
FAMCICLOVIR	250MG	TABLET; ORAL	Prescription	none

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last updated on 11-21-2008

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