NAPROXEN SODIUM Detail

Drug Name(s):
NAPROXEN SODIUM

FDA Application No.:
NDA 075416

Active Ingredient(s):
NAPROXEN SODIUM

Company:
ANDRX PHARMS

Original Approval or Tentative Approval Date:
March 20, 2003

Products on Application NDA 075416:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NAPROXEN SODIUM	EQ 375MG BASE	TABLET, EXTENDED RELEASE; ORAL	Prescription	AB

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January 2009

NAPROXEN SODIUM Detail

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