HALOPERIDOL DECANOATE Detail

Drug Name(s):
HALOPERIDOL DECANOATE

FDA Application No.:
NDA 075176

Active Ingredient(s):
HALOPERIDOL DECANOATE

Company:
MAYNE PHARMA USA

Original Approval or Tentative Approval Date:
February 8, 2000

Products on Application NDA 075176:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
HALOPERIDOL DECANOATE	EQ 50MG BASE/ML	INJECTABLE; INJECTION	Discontinued	none

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January 2009

HALOPERIDOL DECANOATE Detail

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