Fosphenytoin Sodium 68462-0621-54

Package NDC

68462-0621-54

Manufacturer: Glenmark Pharmaceuticals Inc., Usa
Dosage Form: Injection, Solution
Route: Intramuscular And Intravenous
Product Type: Human Prescription Drug
Marketing Start: October 13, 2023
Listing Expires: December 31, 2027
Application: ANDA214926

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Active Ingredients

Ingredient	Strength
Fosphenytoin Sodium	50 mg/mL

Drug Class

Anti-epileptic Agent [EPC]Cytochrome P450 1A2 Inducers [MoA]Cytochrome P450 2B6 Inducers [MoA]

Selected Package

68462-0621-54Selected

25 VIAL, SINGLE-DOSE in 1 CARTON (68462-621-54) / 2 mL in 1 VIAL, SINGLE-DOSE (68462-621-02)