Lacosamide 67877-0735
Product NDC
67877-0735- Manufacturer
- Ascend Laboratories, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CV
- Marketing Start
- April 1, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA214695
Active Ingredients
| Ingredient | Strength |
|---|---|
| Lacosamide | 150 mg/1 |
Drug Class
Decreased Central Nervous System Disorganized Electrical Activity [PE]
Packaging Options(4)
500 TABLET, FILM COATED in 1 BOTTLE (67877-735-05)
6 BLISTER PACK in 1 CARTON (67877-735-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK
60 TABLET, FILM COATED in 1 BOTTLE (67877-735-60)
90 TABLET, FILM COATED in 1 BOTTLE (67877-735-90)