"0517-6902-25" National Drug Code (NDC)

NDC Code	0517-6902-25
Package Description	25 VIAL, SINGLE-DOSE in 1 TRAY (0517-6902-25) > 2 mL in 1 VIAL, SINGLE-DOSE (0517-6902-01)
Product NDC	0517-6902
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Fosphenytoin Sodium
Non-Proprietary Name	Fosphenytoin Sodium
Dosage Form	INJECTION, SOLUTION
Usage	INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date	20100730
Marketing Category Name	ANDA
Application Number	ANDA090099
Manufacturer	American Regent, Inc.
Substance Name	FOSPHENYTOIN 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]