NASALIDE Detail

Drug Name(s):
NASALIDE

FDA Application No.:
NDA 018148

Active Ingredient(s):
FLUNISOLIDE

Company:
IVAX RES

Original Approval or Tentative Approval Date:
August 29, 1983

Products on Application NDA 018148:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
FLUNISOLIDE	0.025MG/SPRAY	SPRAY, METERED; NASAL	Discontinued	none

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last updated on 11-21-2008

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