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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 017247
Company: NOVARTIS

Products on NDA 17247

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
SANOREX	MAZINDOL	1MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET;ORAL	Discontinued	None	Yes	No
SANOREX	MAZINDOL	2MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET;ORAL	Discontinued	None	Yes	No

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