Last Updated: September 24, 2026

Details for New Drug Application (NDA): 017247

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NDA 017247 describes SANOREX, which is a drug marketed by Novartis and is included in one NDA. Additional details are available on the SANOREX profile page.

The generic ingredient in SANOREX is mazindol. There is one drug master file entry for this compound. Additional details are available on the mazindol profile page.

Summary for 017247

Tradename:	SANOREX
Applicant:	Novartis
Ingredient:	mazindol
Patents:	0

Medical Subject Heading (MeSH) Categories for 017247

Adrenergic Uptake Inhibitors
Central Nervous System Stimulants
Dopamine Uptake Inhibitors

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	1MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons
Approval Date:	Approved Prior to Jan 1, 1982	TE:		RLD:	Yes

Profile for product number 002

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	2MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons
Approval Date:	Approved Prior to Jan 1, 1982	TE:		RLD:	Yes

Expired US Patents for NDA 017247

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Novartis	SANOREX	mazindol	TABLET;ORAL	017247-001	Approved Prior to Jan 1, 1982	⤷ Start Trial	⤷ Start Trial
Novartis	SANOREX	mazindol	TABLET;ORAL	017247-002	Approved Prior to Jan 1, 1982	⤷ Start Trial	⤷ Start Trial
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>Patent No.	>Patent Expiration

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