Phenytoin Sodium 51662-1250
Product NDC
51662-1250- 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]
Packaging Options(1)
5 mL in 1 VIAL, SINGLE-DOSE (51662-1250-1)