NDC 47335-918
Lacosamide
Lacosamide
Lacosamide is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is Lacosamide.
| Product ID | 47335-918_5a4a0d47-9ceb-4987-87ef-81ca33259034 |
| NDC | 47335-918 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Lacosamide |
| Generic Name | Lacosamide |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2022-03-19 |
| Marketing Category | ANDA / |
| Application Number | ANDA205031 |
| Labeler Name | Sun Pharmaceutical Industries, Inc. |
| 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 |