Lacosamide 70518-4503
Product NDC
70518-4503- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CV
- Marketing Start
- October 14, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA204974
Active Ingredients
| Ingredient | Strength |
|---|---|
| Lacosamide | 50 mg/1 |
Drug Class
Decreased Central Nervous System Disorganized Electrical Activity [PE]
Packaging Options(1)
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4503-0)