LERITINE Detail

Drug Name(s):
LERITINE

FDA Application No.:
NDA 010585

Active Ingredient(s):
ANILERIDINE HYDROCHLORIDE

Company:
MERCK

Products on Application NDA 010585:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
ANILERIDINE HYDROCHLORIDE	EQ 25MG BASE	TABLET; ORAL	Discontinued	none

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last updated on 11-21-2008

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