ONDANSETRON Detail

Drug Name(s):
ONDANSETRON

FDA Application No.:
NDA 076252

Active Ingredient(s):
ONDANSETRON HYDROCHLORIDE

Company:
TEVA PHARMS

Original Approval or Tentative Approval Date:
March 27, 2006

Products on Application NDA 076252:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
ONDANSETRON HYDROCHLORIDE	24MG	TABLET; ORAL	Tentative approval	none
ONDANSETRON HYDROCHLORIDE	4MG	TABLET; ORAL	Tentative approval	none

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January 2009

ONDANSETRON Detail

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