LAMPRENE Detail

Drug Name(s):
LAMPRENE

FDA Application No.:
NDA 019500

Active Ingredient(s):
CLOFAZIMINE

Company:
NOVARTIS

Original Approval or Tentative Approval Date:
December 14, 1986

Products on Application NDA 019500:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
CLOFAZIMINE	50MG	CAPSULE; ORAL	Prescription	none

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last updated on 11-21-2008

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