"0409-1317-02" National Drug Code (NDC)

NDC Code	0409-1317-02
Package Description	5 TRAY in 1 CONTAINER (0409-1317-02) > 5 AMPULE in 1 TRAY > 5 mL in 1 AMPULE
Product NDC	0409-1317
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Phenytoin Sodium
Non-Proprietary Name	Phenytoin Sodium
Dosage Form	INJECTION, SOLUTION
Usage	INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date	19870317
Marketing Category Name	ANDA
Application Number	ANDA089521
Manufacturer	Hospira, Inc.
Substance Name	PHENYTOIN SODIUM
Strength	50
Strength Unit	mg/mL
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]