HALOPERIDOL Detail

Drug Name(s):
HALOPERIDOL

FDA Application No.:
NDA 072121

Active Ingredient(s):
HALOPERIDOL

Company:
ROYCE LABS

Products on Application NDA 072121:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
HALOPERIDOL	10MG	TABLET; ORAL	Discontinued	none

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last updated on 01-07-2009

HALOPERIDOL Detail

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