Lacosamide 47335-0918
Product NDC
47335-0918- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CV
- Marketing Start
- March 19, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA205031
Active Ingredients
| Ingredient | Strength |
|---|---|
| Lacosamide | 50 mg/1 |
Drug Class
Decreased Central Nervous System Disorganized Electrical Activity [PE]
Packaging Options(3)
1000 TABLET, FILM COATED in 1 BOTTLE (47335-918-18)
180 TABLET, FILM COATED in 1 BOTTLE (47335-918-82)
60 TABLET, FILM COATED in 1 BOTTLE (47335-918-86)