"71699-204-14" National Drug Code (NDC)

NDC Code	71699-204-14
Package Description	14 BLISTER PACK in 1 CARTON (71699-204-14) / 1 TABLET in 1 BLISTER PACK
Product NDC	71699-204
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Xcopri
Non-Proprietary Name	Cenobamate
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20240809
Marketing Category Name	NDA
Application Number	NDA212839
Manufacturer	SK Life Science, Inc.
Substance Name	CENOBAMATE
Strength	12.5
Strength Unit	mg/1
Pharmacy Classes	Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2B6 Inhibitors [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C8 Inducers [MoA], Cytochrome P450 3A Inhibitors [MoA], Cytochrome P450 3A4 Inducers [MoA], GABA A Receptor Positive Modulators [MoA], Sodium Channel Antagonists [MoA]
DEA Schedule	CV