"68084-008-65" National Drug Code (NDC)

NDC Code	68084-008-65
Package Description	5 BLISTER PACK in 1 CARTON (68084-008-65) > 10 CAPSULE in 1 BLISTER PACK (68084-008-11)
Product NDC	68084-008
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Zonisamide
Non-Proprietary Name	Zonisamide
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20130719
End Marketing Date	20160731
Marketing Category Name	ANDA
Application Number	ANDA077636
Manufacturer	American Health Packaging
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]