www.ndcvalidator.com
National Drug Code Lookup | NDC Directory | About | Feedback

"65862-402-39" National Drug Code (NDC)

Divalproex Sodium 3000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-402-39)
(Aurobindo Pharma Limited)

NDC Code65862-402-39
Package Description3000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-402-39)
Product NDC65862-402
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20141024
Marketing Category NameANDA
Application NumberANDA090554
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/65862-402-39





Copyright © 2007-2024 www.ndcvalidator.com