Phenytoin 51672-4069
Product NDC
51672-4069- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Suspension
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 8, 2004
- Listing Expires
- December 31, 2026
- Application
- ANDA040521
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Phenytoin | 125 mg/5mL |
Drug Class
Anti-epileptic Agent [EPC]Anti-epileptic Agent [EPC]Cytochrome P450 1A2 Inducers [MoA]
Packaging Options(2)
237 mL in 1 BOTTLE (51672-4069-1)
1 BOTTLE in 1 CARTON (51672-4069-2) / 237 mL in 1 BOTTLE