"0404-9933-05" National Drug Code (NDC)

NDC Code	0404-9933-05
Package Description	1 VIAL, SINGLE-DOSE in 1 BAG (0404-9933-05) / 5 mL in 1 VIAL, SINGLE-DOSE
Product NDC	0404-9933
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Phenytoin Sodium
Non-Proprietary Name	Phenytoin Sodium
Dosage Form	INJECTION
Usage	INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date	20220113
End Marketing Date	20250131
Marketing Category Name	ANDA
Application Number	ANDA084307
Manufacturer	Henry Schein, Inc.
Substance Name	PHENYTOIN SODIUM
Strength	250
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]