MAXIDEX Detail

Drug Name(s):
MAXIDEX

FDA Application No.:
NDA 083342

Active Ingredient(s):
DEXAMETHASONE SODIUM PHOSPHATE

Company:
ALCON

Original Approval or Tentative Approval Date:
October 22, 1973

Products on Application NDA 083342:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
DEXAMETHASONE SODIUM PHOSPHATE	EQ 0.05% PHOSPHATE	OINTMENT; OPHTHALMIC	Discontinued	none

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last updated on 11-19-2008

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