VASOCON Detail

Drug Name(s):
VASOCON

FDA Application No.:
NDA 080235

Active Ingredient(s):
NAPHAZOLINE HYDROCHLORIDE

Company:
NOVARTIS

Original Approval or Tentative Approval Date:
June 6, 1971

Products on Application NDA 080235:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NAPHAZOLINE HYDROCHLORIDE	0.1%	SOLUTION/DROPS; OPHTHALMIC	Prescription	AT

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last updated on 12-05-2008