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"65862-401-71" National Drug Code (NDC)

Divalproex Sodium 7000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-401-71)
(Aurobindo Pharma Limited)

NDC Code65862-401-71
Package Description7000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-401-71)
Product NDC65862-401
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20110421
Marketing Category NameANDA
Application NumberANDA090554
ManufacturerAurobindo Pharma Limited
Substance NameDIVALPROEX SODIUM
Strength125
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/65862-401-71





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