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Healthtrust
Cerilliant
Deloitte
Julphar
US Army
Chinese Patent Office
Daiichi Sankyo
McKesson
Boehringer Ingelheim

Generated: May 27, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 088521

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NDA 088521 describes PHENYTOIN SODIUM, which is a drug marketed by Aurobindo Pharma Ltd, Pharmeral, Watson Labs, Acella Pharms Llc, Fresenius Kabi Usa, Hospira, Luitpold, Marsam Pharms Llc, Smith And Nephew, Solopak, Warner Chilcott, and West-ward Pharms Int, and is included in sixteen NDAs. It is available from seven suppliers. Additional details are available on the PHENYTOIN SODIUM profile page.

The generic ingredient in PHENYTOIN SODIUM is phenytoin sodium. There are twenty drug master file entries for this compound. Forty suppliers are listed for this compound. Additional details are available on the phenytoin sodium profile page.
Summary for 088521
Tradename:PHENYTOIN SODIUM
Applicant:Smith And Nephew
Ingredient:phenytoin sodium
Patents:0
Therapeutic Class:Anticonvulsants
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:INJECTABLE;INJECTIONStrength50MG/ML
Approval Date:Dec 18, 1984TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Merck
Argus Health
Cipla
Chinese Patent Office
Citi
Daiichi Sankyo
Johnson and Johnson
Fish and Richardson
Mallinckrodt

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