LEFLUNOMIDE Detail

Drug Name(s):
LEFLUNOMIDE

FDA Application No.:
NDA 077086

Active Ingredient(s):
LEFLUNOMIDE

Company:
KALI LABS

Original Approval or Tentative Approval Date:
September 12, 2005

Products on Application NDA 077086:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
LEFLUNOMIDE	20MG	TABLET; ORAL	Prescription	AB

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last updated on 11-19-2008

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