Details for New Drug Application (NDA): 087835

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NDA 087835 describes OXTRIPHYLLINE, which is a drug marketed by Morton Grove and Watson Labs and is included in four NDAs. Additional details are available on the OXTRIPHYLLINE profile page.

The generic ingredient in OXTRIPHYLLINE is oxtriphylline. There are three drug master file entries for this compound. Additional details are available on the oxtriphylline profile page.

Summary for 087835

Tradename:	OXTRIPHYLLINE
Applicant:	Watson Labs
Ingredient:	oxtriphylline
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET, DELAYED RELEASE;ORAL			Strength	200MG
Approval Date:	Aug 25, 1983	TE:		RLD:	No

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