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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 075416
Company: ACTAVIS LABS FL INC

Products on ANDA 75416

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
NAPROXEN SODIUM	NAPROXEN SODIUM	EQ 500MG BASE	TABLET, EXTENDED RELEASE;ORAL	Prescription	AB	No	No
NAPROXEN SODIUM	NAPROXEN SODIUM	EQ 375MG BASE	TABLET, EXTENDED RELEASE;ORAL	Prescription	AB	No	No
NAPROXEN SODIUM	NAPROXEN SODIUM	EQ 750MG BASE	TABLET, EXTENDED RELEASE;ORAL	Prescription	AB	No	No

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