Lacosamide 70518-4689
Product NDC
70518-4689- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CV
- Marketing Start
- July 3, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA214695
Active Ingredients
| Ingredient | Strength |
|---|---|
| Lacosamide | 50 mg/1 |
Drug Class
Decreased Central Nervous System Disorganized Electrical Activity [PE]
Packaging Options(2)
30 POUCH in 1 BOX (70518-4689-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4689-1)
100 POUCH in 1 BOX (70518-4689-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-4689-1)