NAPROXEN SODIUM Detail

Drug Name(s):
NAPROXEN SODIUM

FDA Application No.:
NDA 074195

Active Ingredient(s):
NAPROXEN SODIUM

Company:
WATSON LABS

Original Approval or Tentative Approval Date:
July 12, 1995

Products on Application NDA 074195:

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

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last updated on 12-01-2008

NAPROXEN SODIUM Detail

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