"0615-7764-39" National Drug Code (NDC)

NDC Code	0615-7764-39
Package Description	30 TABLET, CHEWABLE in 1 BLISTER PACK (0615-7764-39)
Product NDC	0615-7764
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Phenytoin
Non-Proprietary Name	Phenytoin
Dosage Form	TABLET, CHEWABLE
Usage	ORAL
Start Marketing Date	20121226
Marketing Category Name	ANDA
Application Number	ANDA200691
Manufacturer	NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name	PHENYTOIN
Strength	50
Strength Unit	mg/1
Pharmacy Classes	Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Cytochrome P450 1A2 Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA],Cytochrome P450 2C8 Inducers [MoA],Cytochrome P450 2C19 Inducers [MoA],Cytochrome P450 2D6 Inducers [MoA],Cytochrome P450 3A Inducers [MoA],Cytochrome P450 2C9 Inducers [MoA]