Details for New Drug Application (NDA): 205237
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The generic ingredient in LACOSAMIDE is lacosamide. There are twenty-two drug master file entries for this compound. Fifty-six suppliers are listed for this compound. Additional details are available on the lacosamide profile page.
Summary for 205237
| Tradename: | LACOSAMIDE |
| Applicant: | Sciegen Pharms Inc |
| Ingredient: | lacosamide |
| Patents: | 0 |
Pharmacology for NDA: 205237
| Physiological Effect | Decreased Central Nervous System Disorganized Electrical Activity |
Suppliers and Packaging for NDA: 205237
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| LACOSAMIDE | lacosamide | TABLET;ORAL | 205237 | ANDA | ScieGen Pharmaceuticals Inc | 50228-192 | 50228-192-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (50228-192-10) |
| LACOSAMIDE | lacosamide | TABLET;ORAL | 205237 | ANDA | ScieGen Pharmaceuticals Inc | 50228-192 | 50228-192-30 | 30 TABLET, FILM COATED in 1 BOTTLE (50228-192-30) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 50MG | ||||
| Approval Date: | Mar 17, 2022 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 100MG | ||||
| Approval Date: | Mar 17, 2022 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 150MG | ||||
| Approval Date: | Mar 17, 2022 | TE: | AB | RLD: | No | ||||
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