LEUSTATIN Detail

Drug Name(s):
LEUSTATIN

FDA Application No.:
NDA 020229

Active Ingredient(s):
CLADRIBINE

Company:
ORTHO BIOTECH

Original Approval or Tentative Approval Date:
February 25, 1993

Products on Application NDA 020229:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
CLADRIBINE	1MG/ML	INJECTABLE; INJECTION	Prescription	AP

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last updated on 11-21-2008

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