"0143-9782-10" National Drug Code (NDC)

NDC Code	0143-9782-10
Package Description	10 VIAL in 1 PACKAGE (0143-9782-10) > 10 mL in 1 VIAL (0143-9782-01)
Product NDC	0143-9782
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	20091202
Marketing Category Name	ANDA
Application Number	ANDA078765
Manufacturer	West-Ward Pharmaceuticals Corp
Substance Name	FOSPHENYTOIN 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]