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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 074319
Company: PUREPAC PHARM

Products on ANDA 074319

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
NAPROXEN SODIUM	NAPROXEN SODIUM	EQ 250MG BASE	TABLET;ORAL	Discontinued	None	No	No
NAPROXEN SODIUM	NAPROXEN SODIUM	EQ 500MG BASE	TABLET;ORAL	Discontinued	None	No	No

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