Drug Details: NAPROXEN SODIUM

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	NAPROXEN SODIUM
FDA Application No:	(NDA) 021920
Active Ingredient(s):	NAPROXEN SODIUM
Company:	BANNER PHARMACAPS
Original Approval or Tentative Approval Date:	February 17, 2006
Chemical Type:	3 New dosage form
Review Classification:	S Standard review drug

There are no Therapeutic Equivalents	Label Information
Approval History, Letters, Reviews and Related Documents

You can see the products in the same application. The table can be sorted by clicking the header columns.

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code
NAPROXEN SODIUM	NAPROXEN SODIUM	EQ 200MG BASE	CAPSULE; ORAL	OTC	Yes	None

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