NAPHCON-A Detail

Drug Name(s):
NAPHCON-A

FDA Application No.:
NDA 020226

Active Ingredient(s):
NAPHAZOLINE HYDROCHLORIDE; PHENIRAMINE MALEATE

Company:
ALCON

Original Approval or Tentative Approval Date:
June 7, 1994

Products on Application NDA 020226:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NAPHAZOLINE HYDROCHLORIDE; PHENIRAMINE MALEATE	0.025%;0.3%	SOLUTION/DROPS; OPHTHALMIC	OTC	none

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last updated on 11-21-2008

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