NAPHAZOLINE HYDROCHLORIDE Detail

Drug Name(s):
NAPHAZOLINE HYDROCHLORIDE

FDA Application No.:
NDA 083590

Active Ingredient(s):
NAPHAZOLINE HYDROCHLORIDE

Company:
TAYLOR

Original Approval or Tentative Approval Date:
August 21, 1974

Products on Application NDA 083590:

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