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Vimpat
Vimpat - 0131-2480-35 - (lacosamide)
Drug Information of Vimpat
| Product NDC: | 0131-2480 |
| Proprietary Name: | Vimpat |
| Non Proprietary Name: | lacosamide |
| Active Ingredient(s): | 200 mg/1 & nbsp; lacosamide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vimpat
| Product NDC: | 0131-2480 |
| Labeler Name: | Kremers Urban Pharmaceuticals Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022253 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090526 |
Package Information of Vimpat
| Package NDC: | 0131-2480-35 |
| Package Description: | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0131-2480-35) |
NDC Information of Vimpat
| NDC Code | 0131-2480-35 |
| Proprietary Name | Vimpat |
| Package Description | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0131-2480-35) |
| Product NDC | 0131-2480 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | lacosamide |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20090526 |
| Marketing Category Name | NDA |
| Labeler Name | Kremers Urban Pharmaceuticals Inc |
| Substance Name | LACOSAMIDE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
