"47335-833-01" National Drug Code (NDC)

NDC Code	47335-833-01
Package Description	25 VIAL, SINGLE-DOSE in 1 CARTON (47335-833-01) > 2 mL in 1 VIAL, SINGLE-DOSE
Product NDC	47335-833
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	20090814
Marketing Category Name	ANDA
Application Number	ANDA078417
Manufacturer	Sun Pharma Global FZE
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]