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Farmers Insurance
US Department of Justice
QuintilesIMS
Johnson and Johnson
Covington
Chinese Patent Office
Cantor Fitzgerald
Fuji
Mallinckrodt
Boehringer Ingelheim

Generated: February 17, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 089070

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NDA 089070 describes PROCAINAMIDE HYDROCHLORIDE, which is a drug marketed by Ascot, Idt Australia Ltd, Ivax Sub Teva Pharms, Lannett, Lederle, Roxane, Vangard, Watson Labs, Abraxis Pharm, Hospira, Intl Medication, Nexus Pharms, Pharmafair, Smith And Nephew, Solopak, Warner Chilcott, West-ward Pharms Int, Ani Pharms Inc, Inwood Labs, and Sandoz, and is included in fifty-eight NDAs. It is available from five suppliers. Additional details are available on the PROCAINAMIDE HYDROCHLORIDE profile page.

The generic ingredient in PROCAINAMIDE HYDROCHLORIDE is procainamide hydrochloride. There are eight drug master file entries for this compound. Five suppliers are listed for this compound. Additional details are available on the procainamide hydrochloride profile page.
Summary for 089070
Tradename:PROCAINAMIDE HYDROCHLORIDE
Applicant:Hospira
Ingredient:procainamide hydrochloride
Patents:0
Therapeutic Class:Cardiovascular Agents
Formulation / Manufacturing:see details
Pharmacology for NDA: 089070
Medical Subject Heading (MeSH) Categories for 089070
Suppliers and Packaging for NDA: 089070
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
PROCAINAMIDE HYDROCHLORIDE procainamide hydrochloride INJECTABLE;INJECTION 089070 ANDA Hospira, Inc. 0409-1903 N 0409-1903-01
PROCAINAMIDE HYDROCHLORIDE procainamide hydrochloride INJECTABLE;INJECTION 089070 ANDA Hospira, Inc. 0409-1903 N 0409-1903-25

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrength500MG/ML
Approval Date:Feb 12, 1986TE:RLD:No

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Cerilliant
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Fish and Richardson
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