"42192-614-03" National Drug Code (NDC)

NDC Code	42192-614-03
Package Description	25 VIAL in 1 CARTON (42192-614-03) > 2 mL in 1 VIAL
Product NDC	42192-614
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Phenytoin Sodium
Non-Proprietary Name	Phenytoin Sodium
Dosage Form	INJECTION
Usage	INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date	20211201
Marketing Category Name	ANDA
Application Number	ANDA040573
Manufacturer	Acella Pharmaceuticals, LLC
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]