"80674-102-25" National Drug Code (NDC)

NDC Code	80674-102-25
Package Description	25 VIAL, SINGLE-USE in 1 CARTON (80674-102-25) / 2 mL in 1 VIAL, SINGLE-USE (80674-102-02)
Product NDC	80674-102
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Sesquient
Non-Proprietary Name	Fosphenytoin Sodium
Dosage Form	INJECTION, SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	20210601
End Marketing Date	20231231
Marketing Category Name	NDA
Application Number	NDA210864
Manufacturer	Sedor Pharmaceuticals, LLC
Substance Name	FOSPHENYTOIN SODIUM
Strength	100
Strength Unit	mg/2mL
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]