NDC 80674-102


Fosphenytoin Sodium

Sesquient is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Sedor Pharmaceuticals, Llc. The primary component is Fosphenytoin Sodium.

Product ID80674-102_8fa2abc6-e2d1-4647-a090-ca2f83481f5f
Product TypeHuman Prescription Drug
Proprietary NameSesquient
Generic NameFosphenytoin Sodium
Dosage FormInjection, Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2021-06-01
Marketing CategoryNDA /
Application NumberNDA210864
Labeler NameSedor Pharmaceuticals, LLC
Active Ingredient Strength100 mg/2mL
Pharm ClassesAnti-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]
NDC Exclude FlagN
Listing Certified Through2021-12-31


NDC 80674-102-25

25 VIAL, SINGLE-USE in 1 CARTON (80674-102-25) > 2 mL in 1 VIAL, SINGLE-USE (80674-102-02)
Marketing Start Date2021-06-01
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Sesquient" or generic name "Fosphenytoin Sodium"

NDCBrand NameGeneric Name
80674-102Sesquientfosphenytoin sodium
80674-210Sesquientfosphenytoin sodium
0069-5471CEREBYXFosphenytoin Sodium
0069-5474CEREBYXFosphenytoin Sodium
0069-6001CEREBYXFosphenytoin Sodium
63323-403FosphenytoinFOSPHENYTOIN SODIUM
0143-9782Fosphenytoin SodiumFosphenytoin Sodium
0143-9788Fosphenytoin SodiumFosphenytoin Sodium
0641-6136Fosphenytoin SodiumFosphenytoin Sodium
0641-6137Fosphenytoin SodiumFosphenytoin Sodium
64679-729FOSPHENYTOIN SODIUMfosphenytoin sodium
64679-730FOSPHENYTOIN SODIUMfosphenytoin sodium
65162-998Fosphenytoin SodiumFosphenytoin Sodium
65162-999Fosphenytoin SodiumFosphenytoin Sodium
67457-516Fosphenytoin SodiumFosphenytoin Sodium
67457-517Fosphenytoin SodiumFosphenytoin Sodium

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