NAPROXEN Detail

Drug Name(s):
NAPROXEN

FDA Application No.:
NDA 074936

Active Ingredient(s):
NAPROXEN

Company:
ACTAVIS ELIZABETH

Original Approval or Tentative Approval Date:
February 23, 1998

Products on Application NDA 074936:

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

Recall Notices

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FDA Announces Class I Recall of Ophthalmic Surgical Device
Stryker Craniomaxillofacial Issues Nationwide Recall of its Custom Cranial Implant Kits; Catalogue Numbers 54-00101, 54-00102, 54-00103 and 54-00104, all lots shipped sterile (December 23)
KRC Food Trading Inc. Recall of Fish Cake Sushi (December 23)

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January 2009

NAPROXEN Detail

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