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Generated: August 21, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 040781

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NDA 040781 describes PHENYTOIN SODIUM, which is a drug marketed by Warner Chilcott, Marsam Pharms Llc, Fresenius Kabi Usa, West-ward Pharms Int, Aurobindo Pharma Ltd, Smith And Nephew, Solopak, Hospira, Watson Labs, Pharmeral, Acella Pharms Llc, and Luitpold, and is included in sixteen NDAs. It is available from eight suppliers. Additional details are available on the PHENYTOIN SODIUM profile page.

The generic ingredient in PHENYTOIN SODIUM is phenytoin sodium. There are nineteen drug master file entries for this compound. Forty-one suppliers are listed for this compound. Additional details are available on the phenytoin sodium profile page.

Summary for NDA: 040781

Tradename:
1
Applicant:
1
Ingredient:
1
Patents:0
Therapeutic Class:Anticonvulsants
Formulation / Manufacturing:see details

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrength50MG/ML
Approval Date:Dec 4, 2007TE:APRLD:No


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Serving 500+ biopharmaceutical companies globally:

Queensland Health
Fish and Richardson
UBS
Merck
Mallinckrodt
Harvard Business School
Medtronic
Boehringer Ingelheim
US Department of Justice
Chubb

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