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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 008402
Company: SANOFI AVENTIS US

Products on NDA 008402

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
PHISOHEX	HEXACHLOROPHENE	3%	EMULSION;TOPICAL	Discontinued	None	No	No

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