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NDC 00078-0456-35 Trileptal 150 mg/1 Details
Trileptal 150 mg/1
Trileptal is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Novartis Pharmaceuticals Corporation. The primary component is OXCARBAZEPINE.
MedlinePlus Drug Summary
Oxcarbazepine (Trileptal) is used alone or in combination with other medications to control certain types of seizures in adults and children. Oxcarbazepine extended-release tablets (Oxtellar XR) are used in combination with other medications to control certain types of seizures in adults and children 6 years of age and older. Oxcarbazepine is in a class of medications called anticonvulsants. It works by decreasing abnormal electrical activity in the brain.
Related Packages: 00078-0456-35Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Oxcarbazepine
Product Information
| NDC | 00078-0456 |
|---|---|
| Product ID | 0078-0456_2201beee-4887-43fa-9343-ac93936b0b90 |
| Associated GPIs | 72600046000310 |
| GCN Sequence Number | 044336 |
| GCN Sequence Number Description | oxcarbazepine TABLET 150 MG ORAL |
| HIC3 | H4B |
| HIC3 Description | ANTICONVULSANTS |
| GCN | 21724 |
| HICL Sequence Number | 011735 |
| HICL Sequence Number Description | OXCARBAZEPINE |
| Brand/Generic | Brand |
| Proprietary Name | Trileptal |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | oxcarbazepine |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 150 |
| Active Ingredient Units | mg/1 |
| Substance Name | OXCARBAZEPINE |
| Labeler Name | Novartis Pharmaceuticals Corporation |
| Pharmaceutical Class | Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE] |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA021014 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00078-0456-35 (00078045635)
| NDC Package Code | 0078-0456-35 |
|---|---|
| Billing NDC | 00078045635 |
| Package | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0078-0456-35) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0078-0456-61) |
| Marketing Start Date | 2000-01-30 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |