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Serving 500+ biopharmaceutical companies globally:

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Generated: August 17, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 078445

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NDA 078445 describes DIVALPROEX SODIUM, which is a drug marketed by Zydus Pharms Usa Inc, G And W Labs Inc, Wockhardt, Mylan, Prinston Inc, Anchen Pharms, Nu Pharm, Aurobindo Pharma Ltd, Amneal Pharms, Teva, Orchid Hlthcare, Dr Reddys Labs Ltd, Unichem Labs Ltd, Reddys, Actavis Labs Fl Inc, Upsher-smith Labs, Lupin, Sandoz, Impax Labs, and Sun Pharm Inds, and is included in thirty NDAs. It is available from forty-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. Fifty-one suppliers are listed for this compound. Additional details are available on the divalproex sodium profile page.

Summary for NDA: 078445

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

Pharmacology for NDA: 078445

Suppliers and Packaging for NDA: 078445

Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
DIVALPROEX SODIUM
divalproex sodium
TABLET, EXTENDED RELEASE;ORAL 078445 ANDA Par Pharmaceutical, Inc. 10370-510 10370-510-10 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (10370-510-10)
DIVALPROEX SODIUM
divalproex sodium
TABLET, EXTENDED RELEASE;ORAL 078445 ANDA Par Pharmaceutical, Inc. 10370-510 10370-510-50 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (10370-510-50)

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET, EXTENDED RELEASE;ORALStrengthEQ 250MG VALPROIC ACID
Approval Date:Feb 26, 2009TE:ABRLD:No

Summary for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET, EXTENDED RELEASE;ORALStrengthEQ 500MG VALPROIC ACID
Approval Date:Aug 4, 2009TE:ABRLD:No


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