TAVIST Detail

Drug Name(s):
TAVIST

FDA Application No.:
NDA 018675

Active Ingredient(s):
CLEMASTINE FUMARATE

Company:
NOVARTIS

Original Approval or Tentative Approval Date:
December 1, 1986

Products on Application NDA 018675:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
CLEMASTINE FUMARATE	EQ 0.5MG BASE/5ML	SYRUP; ORAL	Discontinued	none

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last updated on 11-21-2008

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