Phenytoin Sodium 51662-1250-01

Package NDC

51662-1250-01

Manufacturer: Hf Acquisition Co Llc, Dba Healthfirst
Dosage Form: Injection
Route: Intramuscular And Intravenous
Product Type: Human Prescription Drug
Marketing Start: September 19, 2018
Listing Expires: December 31, 2026
Application: ANDA084307

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Active Ingredients

Ingredient	Strength
Phenytoin Sodium	50 mg/mL

Drug Class

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

Selected Package

51662-1250-01Selected

5 mL in 1 VIAL, SINGLE-DOSE (51662-1250-1)