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Generated: May 20, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 007529

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NDA 007529 describes QUINIDINE GLUCONATE, which is a drug marketed by Lilly, Ascot, Aurolife Pharma Llc, Cycle Pharms Ltd, Halsey, Sun Pharm Industries, Superpharm, and Watson Labs, and is included in nine NDAs. It is available from four suppliers. Additional details are available on the QUINIDINE GLUCONATE profile page.

The generic ingredient in QUINIDINE GLUCONATE is quinidine gluconate. There are twenty-seven drug master file entries for this compound. Four suppliers are listed for this compound. Additional details are available on the quinidine gluconate profile page.
Summary for 007529
Ingredient:quinidine gluconate
Therapeutic Class:Cardiovascular Agents
Formulation / Manufacturing:see details
Pharmacology for NDA: 007529
Suppliers and Packaging for NDA: 007529
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
QUINIDINE GLUCONATE quinidine gluconate INJECTABLE;INJECTION 007529 NDA Eli Lilly and Company 0002-1407 N 0002-1407-01

Profile for product number 002

Active Rx/OTC/Discontinued:DISCNDosage:INJECTABLE;INJECTIONStrength80MG/ML
Approval Date:Feb 10, 1989TE:RLD:Yes

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