"61919-815-71" National Drug Code (NDC)

NDC Code	61919-815-71
Package Description	100 CAPSULE in 1 BOTTLE (61919-815-71)
Product NDC	61919-815
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Phenytoin Sodium
Non-Proprietary Name	Phenytoin Sodium
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20140101
Marketing Category Name	ANDA
Application Number	ANDA040765
Manufacturer	DIRECT RX
Substance Name	PHENYTOIN SODIUM
Strength	100
Strength Unit	mg/1
Pharmacy Classes	Anti-epileptic Agent [EPC], Cytochrome P450 1A2 Inducers [MoA], Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C19 Inducers [MoA], Cytochrome P450 2C8 Inducers [MoA], Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 2D6 Inducers [MoA], Cytochrome P450 3A Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE]