Fosphenytoin Sodium 68462-0621
Product NDC
68462-0621- 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]
Packaging Options(1)
25 VIAL, SINGLE-DOSE in 1 CARTON (68462-621-54) / 2 mL in 1 VIAL, SINGLE-DOSE (68462-621-02)