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Julphar
Accenture
Moodys
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Healthtrust
Teva
Chinese Patent Office
UBS
McKinsey
Cerilliant

Generated: February 20, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 090099

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NDA 090099 describes FOSPHENYTOIN SODIUM, which is a drug marketed by Amneal Pharms Co, Apotex Inc, Fresenius Kabi Usa, Hikma Farmaceutica, Hospira, Luitpold, Mylan Labs Ltd, Sun Pharma Global, Teva Pharms Usa, West-ward Pharms Int, and Wockhardt, and is included in thirteen NDAs. It is available from seven suppliers. Additional details are available on the FOSPHENYTOIN SODIUM profile page.

The generic ingredient in FOSPHENYTOIN SODIUM is fosphenytoin sodium. There are seven drug master file entries for this compound. Eight suppliers are listed for this compound. Additional details are available on the fosphenytoin sodium profile page.
Summary for 090099
Tradename:FOSPHENYTOIN SODIUM
Applicant:Luitpold
Ingredient:fosphenytoin sodium
Patents:0
Therapeutic Class:Anticonvulsants
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrengthEQ 50MG PHENYTOIN NA/ML
Approval Date:May 13, 2010TE:APRLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

US Department of Justice
Fish and Richardson
Dow
Queensland Health
Teva
Julphar
Healthtrust
Farmers Insurance
Argus Health

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