Phenytoin Sodium 42192-0614
Product NDC
42192-0614- Manufacturer
- Acella Pharmaceuticals, Llc
- Dosage Form
- Injection
- Route
- Intramuscular And Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- December 1, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA040573
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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]
Packaging Options(2)
10 VIAL in 1 CARTON (42192-614-10) / 2 mL in 1 VIAL
10 VIAL in 1 CARTON (42192-614-30) / 5 mL in 1 VIAL