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"65862-594-99" National Drug Code (NDC)

Divalproex Sodium 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-99)
(Aurobindo Pharma Limited)

NDC Code65862-594-99
Package Description1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-99)
Product NDC65862-594
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20140602
Marketing Category NameANDA
Application NumberANDA202419
ManufacturerAurobindo Pharma Limited
Substance NameDIVALPROEX SODIUM
Strength250
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]

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