Phenytoin Sodium 00641-6139
Product NDC
00641-6139- Manufacturer
- Hikma Pharmaceuticals Usa Inc.
- Dosage Form
- Injection
- Route
- Intramuscular And Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- July 16, 1975
- 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]
Packaging Options(2)
10 VIAL in 1 CARTON (0641-6139-10) / 5 mL in 1 VIAL (0641-6139-01)
25 VIAL in 1 CARTON (0641-6139-25) / 5 mL in 1 VIAL (0641-6139-01)