"57237-047-01" National Drug Code (NDC)

NDC Code	57237-047-01
Package Description	100 TABLET, DELAYED RELEASE in 1 BOTTLE (57237-047-01)
Product NDC	57237-047
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	250
Strength Unit	mg/1
Pharmacy Classes	Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]