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Serving hundreds of leading biopharmaceutical companies globally:

Cantor Fitzgerald
Merck
Express Scripts
Harvard Business School
Julphar
Boehringer Ingelheim
Fish and Richardson
Queensland Health
Medtronic

Generated: April 24, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 077254

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NDA 077254 describes DIVALPROEX SODIUM, which is a drug marketed by Dr Reddys Labs Ltd, Mylan, Zydus Pharms Usa Inc, Actavis Labs Fl Inc, Anchen Pharms, Aurobindo Pharma Ltd, Lupin, Nu Pharm, Orchid Hlthcare, Prinston Inc, Sandoz, Sun Pharm Inds, Teva, Unichem Labs Ltd, Upsher-smith Labs, Wockhardt, Amneal Pharms, G And W Labs Inc, Impax Labs, and Reddys, and is included in thirty NDAs. It is available from thirty-eight suppliers. Additional details are available on the DIVALPROEX SODIUM profile page.

The generic ingredient in DIVALPROEX SODIUM is divalproex sodium. There are seventeen drug master file entries for this compound. Forty-one suppliers are listed for this compound. Additional details are available on the divalproex sodium profile page.
Summary for 077254
Tradename:DIVALPROEX SODIUM
Applicant:Mylan
Ingredient:divalproex sodium
Patents:0
Therapeutic Class:Anticonvulsants
Antimigraine Agents
Bipolar Agents
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET, DELAYED RELEASE;ORALStrengthEQ 125MG VALPROIC ACID
Approval Date:Jul 29, 2008TE:RLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:DISCNDosage:TABLET, DELAYED RELEASE;ORALStrengthEQ 250MG VALPROIC ACID
Approval Date:Jul 29, 2008TE:RLD:No

Profile for product number 003

Active Rx/OTC/Discontinued:DISCNDosage:TABLET, DELAYED RELEASE;ORALStrengthEQ 500MG VALPROIC ACID
Approval Date:Jul 29, 2008TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Merck
Express Scripts
McKesson
Farmers Insurance
Johnson and Johnson
Accenture
Cantor Fitzgerald
QuintilesIMS
Colorcon

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