"70121-1390-7" National Drug Code (NDC)

NDC Code	70121-1390-7
Package Description	10 VIAL in 1 CARTON (70121-1390-7) / 10 mL in 1 VIAL (70121-1390-1)
Product NDC	70121-1390
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Fosphenytoin Sodium
Non-Proprietary Name	Fosphenytoin
Dosage Form	INJECTION
Usage	INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date	20160811
Marketing Category Name	ANDA
Application Number	ANDA078476
Manufacturer	Amneal Pharmaceuticals 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]