Product NDC: | 0131-2470 |
Proprietary Name: | Vimpat |
Non Proprietary Name: | lacosamide |
Active Ingredient(s): | & nbsp; lacosamide |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0131-2470 |
Labeler Name: | Kremers Urban Pharmaceuticals Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022253 |
Marketing Category: | NDA |
Start Marketing Date: | 20090526 |
Package NDC: | 0131-2470-99 |
Package Description: | 1 BLISTER PACK in 1 CARTON (0131-2470-99) > 1 KIT in 1 BLISTER PACK |
NDC Code | 0131-2470-99 |
Proprietary Name | Vimpat |
Package Description | 1 BLISTER PACK in 1 CARTON (0131-2470-99) > 1 KIT in 1 BLISTER PACK |
Product NDC | 0131-2470 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | lacosamide |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20090526 |
Marketing Category Name | NDA |
Labeler Name | Kremers Urban Pharmaceuticals Inc |
Substance Name | |
Strength Number | |
Strength Unit | |
Pharmaceutical Classes |