"0071-0369-32" National Drug Code (NDC)

NDC Code	0071-0369-32
Package Description	1000 CAPSULE in 1 BOTTLE (0071-0369-32)
Product NDC	0071-0369
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Dilantin
Non-Proprietary Name	Extended Phenytoin Sodium
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	19760827
Marketing Category Name	ANDA
Application Number	ANDA084349
Manufacturer	Parke-Davis Div of Pfizer Inc
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]