Perampanel 51672-4208
Product NDC
51672-4208- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIII
- Marketing Start
- November 25, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA209538
Active Ingredients
| Ingredient | Strength |
|---|---|
| Perampanel | 10 mg/1 |
Drug Class
Noncompetitive AMPA Glutamate Receptor Antagonist [EPC]AMPA Receptor Antagonists [MoA]Cytochrome P450 2C8 Inhibitors [MoA]
Packaging Options(2)
3 BLISTER PACK in 1 CARTON (51672-4208-2) / 10 TABLET, FILM COATED in 1 BLISTER PACK
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51672-4208-6)