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

"68001-554-03" National Drug Code (NDC)

Divalproex Sodium 500 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-554-03)
(BluePoint Laboratories)

NDC Code68001-554-03
Package Description500 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-554-03)
Product NDC68001-554
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20220810
Marketing Category NameANDA
Application NumberANDA078597
ManufacturerBluePoint Laboratories
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/68001-554-03





Copyright © 2007-2024 www.ndcvalidator.com