"64720-256-10" National Drug Code (NDC)

NDC Code	64720-256-10
Package Description	100 TABLET in 1 BOTTLE, PLASTIC (64720-256-10)
Product NDC	64720-256
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Felbamate
Non-Proprietary Name	Felbamate
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20170306
End Marketing Date	20190430
Marketing Category Name	ANDA
Application Number	ANDA202284
Manufacturer	CorePharma, LLC
Substance Name	FELBAMATE
Strength	600
Strength Unit	mg/1
Pharmacy Classes	Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]