"0071-2214-35" National Drug Code (NDC)

NDC Code	0071-2214-35
Package Description	1 BOTTLE, PLASTIC in 1 CARTON (0071-2214-35) / 237 mL in 1 BOTTLE, PLASTIC
Product NDC	0071-2214
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Dilantin-125
Non-Proprietary Name	Phenytoin
Dosage Form	SUSPENSION
Usage	ORAL
Start Marketing Date	19530106
End Marketing Date	20250331
Marketing Category Name	NDA
Application Number	NDA008762
Manufacturer	Parke-Davis Div of Pfizer Inc
Substance Name	PHENYTOIN
Strength	125
Strength Unit	mg/5mL
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]