NAPROXEN SODIUM Detail

Drug Name(s):
NAPROXEN SODIUM

FDA Application No.:
NDA 074646

Active Ingredient(s):
NAPROXEN SODIUM

Company:
SANDOZ

Original Approval or Tentative Approval Date:
January 12, 1997

Products on Application NDA 074646:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NAPROXEN SODIUM	EQ 200MG BASE	TABLET; ORAL	OTC	none

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last updated on 12-01-2008

NAPROXEN SODIUM Detail

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