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

"65862-401-10" National Drug Code (NDC)

Divalproex Sodium 10 BLISTER PACK in 1 CARTON (65862-401-10) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
(Aurobindo Pharma Limited)

NDC Code65862-401-10
Package Description10 BLISTER PACK in 1 CARTON (65862-401-10) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
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/65862-401-10





Copyright © 2007-2024 www.ndcvalidator.com