"50268-752-15" National Drug Code (NDC)

NDC Code	50268-752-15
Package Description	50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-752-15) > 1 TABLET in 1 BLISTER PACK (50268-752-11)
Product NDC	50268-752
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Topiramate
Non-Proprietary Name	Topiramate
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20140917
End Marketing Date	20181101
Marketing Category Name	ANDA
Application Number	ANDA079162
Manufacturer	AvPAK
Substance Name	TOPIRAMATE
Strength	100
Strength Unit	mg/1
Pharmacy Classes	Decreased Central Nervous System Disorganized Electrical Activity [PE],Cytochrome P450 3A4 Inducers [MoA],Cytochrome P450 2C19 Inhibitors [MoA]