Details for New Drug Application (NDA): 020707

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NDA 020707 describes SKELID, which is a drug marketed by Sanofi Aventis Us and is included in one NDA. Additional details are available on the SKELID profile page.

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

Summary for 020707

Tradename:	SKELID
Applicant:	Sanofi Aventis Us
Ingredient:	tiludronate disodium
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	EQ 200MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons
Approval Date:	Mar 7, 1997	TE:		RLD:	Yes

Expired US Patents for NDA 020707

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Sanofi Aventis Us	SKELID	tiludronate disodium	TABLET;ORAL	020707-001	Mar 7, 1997	⤷ Sign Up	⤷ Sign Up
Sanofi Aventis Us	SKELID	tiludronate disodium	TABLET;ORAL	020707-001	Mar 7, 1997	⤷ Sign Up	⤷ Sign Up
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>Patent No.	>Patent Expiration

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