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"68001-556-00" National Drug Code (NDC)
Divalproex Sodium 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-556-00)
(BluePoint Laboratories)
NDC Code
68001-556-00
Package Description
100 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-556-00)
Product NDC
68001-556
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Divalproex Sodium
Non-Proprietary Name
Divalproex Sodium
Dosage Form
TABLET, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20220810
Marketing Category Name
ANDA
Application Number
ANDA078597
Manufacturer
BluePoint Laboratories
Substance Name
DIVALPROEX SODIUM
Strength
500
Strength Unit
mg/1
Pharmacy Classes
Anti-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/68001-556-00