FLAREX Detail

Drug Name(s):
FLAREX

FDA Application No.:
NDA 019079

Active Ingredient(s):
FLUOROMETHOLONE ACETATE

Company:
ALCON

Original Approval or Tentative Approval Date:
February 10, 1986

Products on Application NDA 019079:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
FLUOROMETHOLONE ACETATE	0.1%	SUSPENSION/DROPS; OPHTHALMIC	Prescription	none

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last updated on 11-21-2008

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