ZOFRAN Detail

Drug Name(s):
ZOFRAN

FDA Application No.:
NDA 020007

Active Ingredient(s):
ONDANSETRON HYDROCHLORIDE

Company:
GLAXOSMITHKLINE

Original Approval or Tentative Approval Date:
February 1, 1993

Products on Application NDA 020007:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
ONDANSETRON HYDROCHLORIDE	EQ 2MG BASE/ML	INJECTABLE; INJECTION	Prescription	none

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last updated on 11-21-2008

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