NAPROXEN Detail

Drug Name(s):
NAPROXEN

FDA Application No.:
NDA 074211

Active Ingredient(s):
NAPROXEN

Company:
ROXANE

Original Approval or Tentative Approval Date:
January 12, 1995

Products on Application NDA 074211:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NAPROXEN	375MG	TABLET; ORAL	Discontinued	none

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last updated on 01-07-2009

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