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Serving hundreds of leading biopharmaceutical companies globally:

Cantor Fitzgerald
Cipla
Harvard Business School
Federal Trade Commission
Merck
Colorcon
Farmers Insurance
US Department of Justice
Daiichi Sankyo

Generated: May 26, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 081031

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NDA 081031 describes QUINIDINE SULFATE, which is a drug marketed by Lilly, G And W Labs Inc, Barr, Contract Pharmacal, Cycle Pharms Ltd, Dava Pharms Inc, Elkins Sinn, Everylife, Halsey, Hikma Pharms, Impax Labs, Ivax Sub Teva Pharms, King Pharms, Kv Pharm, Lannett, 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 three suppliers. Additional details are available on the QUINIDINE SULFATE profile page.

The generic ingredient in QUINIDINE SULFATE is quinidine sulfate. There are twenty-seven drug master file entries for this compound. Three suppliers are 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
Therapeutic Class:Cardiovascular Agents
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength300MG
Approval Date:Apr 14, 1989TE:ABRLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Fish and Richardson
Moodys
QuintilesIMS
Mallinckrodt
Deloitte
Federal Trade Commission
AstraZeneca
Fuji
Queensland Health

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