"57237-136-60" National Drug Code (NDC)

NDC Code	57237-136-60
Package Description	60 TABLET, FILM COATED in 1 BOTTLE (57237-136-60)
Product NDC	57237-136
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Topiramate
Non-Proprietary Name	Topiramate
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20090327
Marketing Category Name	ANDA
Application Number	ANDA078462
Manufacturer	Citron Pharma LLC
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]