"50268-815-15" National Drug Code (NDC)

NDC Code	50268-815-15
Package Description	50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-815-15) > 1 CAPSULE in 1 BLISTER PACK (50268-815-11)
Product NDC	50268-815
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Zonisamide
Non-Proprietary Name	Zonisamide
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20051222
Marketing Category Name	ANDA
Application Number	ANDA077636
Manufacturer	AvPAK
Substance Name	ZONISAMIDE
Strength	100
Strength Unit	mg/1
Pharmacy Classes	Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Sulfonamides [Chemical/Ingredient],Carbonic Anhydrase Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA]