Fosphenytoin Sodium 00143-9782
Product NDC
00143-9782- Manufacturer
- West-Ward Pharmaceuticals Corp
- Dosage Form
- Injection, Solution
- Route
- Intramuscular And Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- December 2, 2009
- Listing Expires
- December 31, 2026
- Application
- ANDA078765
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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]
Packaging Options(1)
10 VIAL in 1 PACKAGE (0143-9782-10) / 10 mL in 1 VIAL (0143-9782-01)