"68788-7351-9" National Drug Code (NDC)

NDC Code	68788-7351-9
Package Description	90 TABLET, FILM COATED in 1 BOTTLE (68788-7351-9)
Product NDC	68788-7351
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Topiramate
Non-Proprietary Name	Topiramate
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20190227
Marketing Category Name	ANDA
Application Number	ANDA078235
Manufacturer	Preferred Pharmaceuticals Inc.
Substance Name	TOPIRAMATE
Strength	50
Strength Unit	mg/1
Pharmacy Classes	Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 3A4 Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE]