Details for New Drug Application (NDA): 017535

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NDA 017535 describes LORELCO, which is a drug marketed by Sanofi Aventis Us and is included in one NDA. Additional details are available on the LORELCO profile page.

The generic ingredient in LORELCO is probucol. There are six drug master file entries for this compound. Additional details are available on the probucol profile page.

Summary for 017535

Tradename:	LORELCO
Applicant:	Sanofi Aventis Us
Ingredient:	probucol
Patents:	0

Medical Subject Heading (MeSH) Categories for 017535

Anticholesteremic Agents
Antioxidants

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	250MG
Approval Date:	Approved Prior to Jan 1, 1982	TE:		RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	500MG
Approval Date:	Jul 6, 1988	TE:		RLD:	No

Expired US Patents for NDA 017535

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Sanofi Aventis Us	LORELCO	probucol	TABLET;ORAL	017535-001	Approved Prior to Jan 1, 1982	⤷ Sign Up	⤷ Sign Up
Sanofi Aventis Us	LORELCO	probucol	TABLET;ORAL	017535-002	Jul 6, 1988	⤷ Sign Up	⤷ Sign Up
Sanofi Aventis Us	LORELCO	probucol	TABLET;ORAL	017535-001	Approved Prior to Jan 1, 1982	⤷ Sign Up	⤷ Sign Up
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>Patent No.	>Patent Expiration

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