Last Updated: September 24, 2026

Details for New Drug Application (NDA): 081031

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NDA 081031 describes QUINIDINE SULFATE, which is a drug marketed by Lilly, Cosette Pharms Nc, Barr, Chartwell Molecular, Chartwell Rx, Contract Pharmacal, Cycle, Dava Pharms Inc, Elkins Sinn, Epic Pharma Llc, Everylife, Halsey, Hikma, Impax Labs, Ivax Sub Teva Pharms, King Pharms, Kv Pharm, Lederle, Perrigo, Pharmavite, Purepac Pharm, Sandoz, Scherer Labs, Sun Pharm Industries, Superpharm, Usl Pharma, Valeant Pharm Intl, Vangard, Vintage Pharms, Warner Chilcott, Watson Labs, and Whiteworth Town Plsn, and is included in forty NDAs. It is available from one supplier. Additional details are available on the QUINIDINE SULFATE profile page.

The generic ingredient in QUINIDINE SULFATE is quinidine sulfate. There is one drug master file entry for this compound. One supplier is listed for this compound. Additional details are available on the quinidine sulfate profile page.

Summary for 081031

Tradename:	QUINIDINE SULFATE
Applicant:	Sun Pharm Industries
Ingredient:	quinidine sulfate
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	300MG
Approval Date:	Apr 14, 1989	TE:		RLD:	No

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