"51662-1251-3" National Drug Code (NDC)

NDC Code	51662-1251-3
Package Description	25 POUCH in 1 BOX (51662-1251-3) / 1 VIAL in 1 POUCH (51662-1251-2) / 2 mL in 1 VIAL
Product NDC	51662-1251
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Phenytoin Sodium
Non-Proprietary Name	Phenytoin Sodium
Dosage Form	INJECTION
Usage	INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date	20180916
Marketing Category Name	ANDA
Application Number	ANDA084307
Manufacturer	HF Acquisition Co LLC, DBA HealthFirst
Substance Name	PHENYTOIN SODIUM
Strength	50
Strength Unit	mg/mL
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]