EC-NAPROSYN Detail

Drug Name(s):
EC-NAPROSYN

FDA Application No.:
NDA 020067

Active Ingredient(s):
NAPROXEN

Company:
ROCHE PALO

Original Approval or Tentative Approval Date:
October 13, 1994

Products on Application NDA 020067:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NAPROXEN	500MG	TABLET, DELAYED RELEASE; ORAL	Prescription	AB

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last updated on 11-21-2008

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