NAPROXEN SODIUM Detail

Drug Name(s):
NAPROXEN SODIUM

FDA Application No.:
NDA 074162

Active Ingredient(s):
NAPROXEN SODIUM

Company:
SANDOZ

Original Approval or Tentative Approval Date:
December 20, 1993

Products on Application NDA 074162:

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

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last updated on 12-01-2008

NAPROXEN SODIUM Detail

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