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"57237-106-05" National Drug Code (NDC)
Divalproex Sodium 500 TABLET, DELAYED RELEASE in 1 BOTTLE (57237-106-05)
(Rising Pharma Holdings, Inc.)
NDC Code
57237-106-05
Package Description
500 TABLET, DELAYED RELEASE in 1 BOTTLE (57237-106-05)
Product NDC
57237-106
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
20141024
Marketing Category Name
ANDA
Application Number
ANDA090554
Manufacturer
Rising Pharma Holdings, Inc.
Substance Name
DIVALPROEX SODIUM
Strength
125
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/57237-106-05