NAPROXEN Detail

Drug Name(s):
NAPROXEN

FDA Application No.:
NDA 074410

Active Ingredient(s):
NAPROXEN

Company:
CLONMEL HLTHCARE

Original Approval or Tentative Approval Date:
March 3, 1997

Products on Application NDA 074410:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NAPROXEN	250MG	TABLET; ORAL	Prescription	AB
NAPROXEN	500MG	TABLET; ORAL	Prescription	AB

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January 2009

NAPROXEN Detail

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