HALOPERIDOL Detail

Drug Name(s):
HALOPERIDOL

FDA Application No.:
NDA 073364

Active Ingredient(s):
HALOPERIDOL LACTATE

Company:
SILARX

Original Approval or Tentative Approval Date:
July 26, 1998

Products on Application NDA 073364:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
HALOPERIDOL LACTATE	EQ 2MG BASE/ML	CONCENTRATE; ORAL	Prescription	AA

Recall Notices

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KRC Food Trading Inc. Recall of Fish Cake Sushi (December 23)

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January 2009

HALOPERIDOL Detail

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