"0071-2214-20" National Drug Code (NDC)

NDC Code	0071-2214-20
Package Description	237 mL in 1 BOTTLE, GLASS (0071-2214-20)
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
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],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]