"72789-004-21" National Drug Code (NDC)

NDC Code	72789-004-21
Package Description	21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-004-21)
Product NDC	72789-004
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Topiramate
Non-Proprietary Name	Topiramate
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20141215
Marketing Category Name	ANDA
Application Number	ANDA090278
Manufacturer	PD-Rx Pharmaceuticals, Inc.
Substance Name	TOPIRAMATE
Strength	100
Strength Unit	mg/1
Pharmacy Classes	Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 3A4 Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE]