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

"68382-315-01" National Drug Code (NDC)

Divalproex Sodium 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-315-01)
(Zydus Pharmaceuticals USA Inc)

NDC Code68382-315-01
Package Description100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-315-01)
Product NDC68382-315
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Proprietary Name SuffixExtended Release
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20130812
End Marketing Date20200130
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA021168
ManufacturerZydus Pharmaceuticals USA Inc
Substance NameDIVALPROEX SODIUM
Strength500
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/68382-315-01





Copyright © 2007-2024 www.ndcvalidator.com