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NDC 70710-1359-06 LACOSAMIDE 10 mg/mL Details
LACOSAMIDE 10 mg/mL
LACOSAMIDE is a INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals USA Inc.. The primary component is LACOSAMIDE.
MedlinePlus Drug Summary
Lacosamide injection is used to control partial onset seizures (seizures that involve only one part of the brain) in adults and children 1 month of age and older who cannot take oral medications. Lacosamide injection is also used in combination with other medications to control primary generalized tonic-clonic seizures (formerly known as a grand mal seizure; seizure that involves the entire body) in adults and children 4 years of age and older who cannot take oral medications. Lacosamide injection is in a class of medications called anticonvulsants. It works by decreasing abnormal electrical activity in the brain.
Related Packages: 70710-1359-06Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Lacosamide Injection
Product Information
| NDC | 70710-1359 |
|---|---|
| Product ID | 70710-1359_be197211-9535-43ec-af98-4318fee3eb82 |
| Associated GPIs | |
| GCN Sequence Number | 064437 |
| GCN Sequence Number Description | lacosamide VIAL 200MG/20ML INTRAVEN |
| HIC3 | H4B |
| HIC3 Description | ANTICONVULSANTS |
| GCN | 14344 |
| HICL Sequence Number | 035872 |
| HICL Sequence Number Description | LACOSAMIDE |
| Brand/Generic | Generic |
| Proprietary Name | LACOSAMIDE |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Lacosamide |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 10 |
| Active Ingredient Units | mg/mL |
| Substance Name | LACOSAMIDE |
| Labeler Name | Zydus Pharmaceuticals USA Inc. |
| Pharmaceutical Class | Decreased Central Nervous System Disorganized Electrical Activity [PE] |
| DEA Schedule | CV |
| Marketing Category | ANDA |
| Application Number | ANDA209465 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70710-1359-06 (70710135906)
| NDC Package Code | 70710-1359-6 |
|---|---|
| Billing NDC | 70710135906 |
| Package | 10 VIAL in 1 CARTON (70710-1359-6) / 20 mL in 1 VIAL (70710-1359-1) |
| Marketing Start Date | 2022-06-29 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |