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Generated: February 18, 2019

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Details for New Drug Application (NDA): 084549

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NDA 084549 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 two 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. Two suppliers are listed for this compound. Additional details are available on the quinidine sulfate profile page.
Summary for 084549
Applicant:Ivax Sub Teva Pharms
Ingredient:quinidine sulfate
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength200MG
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No

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