PATANOL Detail

Drug Name(s):
PATANOL

FDA Application No.:
NDA 020688

Active Ingredient(s):
OLOPATADINE HYDROCHLORIDE

Company:
ALCON

Original Approval or Tentative Approval Date:
December 17, 1996

Products on Application NDA 020688:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
OLOPATADINE HYDROCHLORIDE	EQ 0.1% BASE	SOLUTION/DROPS; OPHTHALMIC	Prescription	none

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last updated on 11-21-2008

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