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"61919-648-30" National Drug Code (NDC)
Divalproex Sodium 30 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-648-30)
(DIRECT RX)
NDC Code
61919-648-30
Package Description
30 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-648-30)
Product NDC
61919-648
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
20140101
Marketing Category Name
ANDA
Application Number
ANDA078597
Manufacturer
DIRECT RX
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/61919-648-30