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Serving leading biopharmaceutical companies globally:

Chubb
Federal Trade Commission
Johnson and Johnson
US Army
Covington
Merck
Daiichi Sankyo
Cerilliant
Colorcon
AstraZeneca

Generated: February 22, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 018832

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NDA 018832 describes ALLOPURINOL, which is a drug marketed by Accord Hlthcare, Apotex Inc, Fosun Pharma, Indoco Remedies, Ipca Labs Ltd, Mutual Pharm, Mylan, Northstar Hlthcare, Puracap Pharm, Purepac Pharm, Sandoz, Sun Pharm Inds Inc, Sun Pharm Industries, Superpharm, Vintage Pharms, Watson Labs, Zydus Pharms Usa Inc, and West-ward Pharms Int, and is included in twenty-five NDAs. It is available from forty-four suppliers. Additional details are available on the ALLOPURINOL profile page.

The generic ingredient in ALLOPURINOL is allopurinol sodium. There are twenty-one drug master file entries for this compound. Two suppliers are listed for this compound. Additional details are available on the allopurinol sodium profile page.
Summary for 018832
Tradename:ALLOPURINOL
Applicant:Watson Labs
Ingredient:allopurinol
Patents:0
Therapeutic Class:Antigout Agents
Formulation / Manufacturing:see details
Pharmacology for NDA: 018832
Mechanism of ActionXanthine Oxidase Inhibitors
Medical Subject Heading (MeSH) Categories for 018832
Suppliers and Packaging for NDA: 018832
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
ALLOPURINOL allopurinol TABLET;ORAL 018832 NDA Actavis Pharma, Inc. 0591-5543 N 0591-5543-10
ALLOPURINOL allopurinol TABLET;ORAL 018832 NDA Actavis Pharma, Inc. 0591-5543 N 0591-5543-01

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength100MG
Approval Date:Sep 28, 1984TE:ABRLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Colorcon
Baxter
Accenture
US Department of Justice
Queensland Health
Fish and Richardson
Boehringer Ingelheim
Cerilliant
Johnson and Johnson

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