Last Updated: November 10, 2026

Details for New Drug Application (NDA): 087785

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NDA 087785 describes QUINIDINE GLUCONATE, which is a drug marketed by Lilly, Adaptis, Ani Pharms, Ascot, Cycle, Halsey, Rising, Sun Pharm Industries, Superpharm, and Watson Labs, and is included in ten NDAs. It is available from three suppliers. Additional details are available on the QUINIDINE GLUCONATE profile page.

The generic ingredient in QUINIDINE GLUCONATE is quinidine gluconate. There is one drug master file entry for this compound. Three suppliers are listed for this compound. Additional details are available on the quinidine gluconate profile page.

Summary for 087785

Tradename:	QUINIDINE GLUCONATE
Applicant:	Watson Labs
Ingredient:	quinidine gluconate
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET, EXTENDED RELEASE;ORAL			Strength	324MG
Approval Date:	Jan 24, 1983	TE:		RLD:	No

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