"68788-8967-9" National Drug Code (NDC)

NDC Code	68788-8967-9
Package Description	90 TABLET, FILM COATED in 1 BOTTLE (68788-8967-9)
Product NDC	68788-8967
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Topiramate
Non-Proprietary Name	Topiramate
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20160111
Marketing Category Name	ANDA
Application Number	ANDA077627
Manufacturer	Preferred Pharmaceuticals Inc.
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]