NAPROXEN Detail

Drug Name(s):
NAPROXEN

FDA Application No.:
NDA 074201

Active Ingredient(s):
NAPROXEN

Company:
TEVA

Original Approval or Tentative Approval Date:
December 20, 1993

Products on Application NDA 074201:

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

Recall Notices

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January 2009

NAPROXEN Detail

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