"64679-729-01" National Drug Code (NDC)

NDC Code	64679-729-01
Package Description	25 VIAL in 1 CARTON (64679-729-01) > 2 mL in 1 VIAL (64679-729-02)
Product NDC	64679-729
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Fosphenytoin Sodium
Non-Proprietary Name	Fosphenytoin Sodium
Dosage Form	INJECTION
Usage	INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date	20070806
Marketing Category Name	ANDA
Application Number	ANDA078137
Manufacturer	Wockhardt USA LLC.
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]