NDC 68462-678
lacosamide
Lacosamide
lacosamide is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Glenmark Pharmaceuticals Inc. Usa. The primary component is Lacosamide.
| Product ID | 68462-678_be80639c-d435-4543-9e58-2f447fe00787 |
| NDC | 68462-678 |
| Product Type | Human Prescription Drug |
| Proprietary Name | lacosamide |
| Generic Name | Lacosamide |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2022-03-18 |
| Marketing Category | ANDA / |
| Application Number | ANDA205006 |
| Labeler Name | Glenmark Pharmaceuticals Inc. USA |
| Substance Name | LACOSAMIDE |
| Active Ingredient Strength | 50 mg/1 |
| Pharm Classes | Decreased Central Nervous System Disorganized Electrical Activity [PE] |
| DEA Schedule | CV |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |