TEGISON Detail

Drug Name(s):
TEGISON

FDA Application No.:
NDA 019369

Active Ingredient(s):
ETRETINATE

Company:
ROCHE

Original Approval or Tentative Approval Date:
September 29, 1986

Products on Application NDA 019369:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
ETRETINATE	10MG	CAPSULE; ORAL	Discontinued	none

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last updated on 11-21-2008

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