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NDC 61919-0883-30 TOPIRAMATE 25 mg/1 Details
TOPIRAMATE 25 mg/1
TOPIRAMATE is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Direct_Rx. The primary component is TOPIRAMATE.
MedlinePlus Drug Summary
Topiramate is used alone or with other medications to treat certain types of seizures including primary generalized tonic-clonic seizures (formerly known as a grand mal seizure; seizure that involves the entire body) and partial onset seizures (seizures that involve only one part of the brain). Topiramate is also used with other medications to control seizures in people who have Lennox-Gastaut syndrome (a disorder that causes seizures and developmental delays). Topiramate is also used to prevent migraine headaches but not to relieve the pain of migraine headaches when they occur. Topiramate is in a class of medications called anticonvulsants. It works by decreasing abnormal excitement in the brain.
Related Packages: 61919-0883-30Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Topiramate
Product Information
| NDC | 61919-0883 |
|---|---|
| Product ID | 61919-883_f6f310b7-a1ea-182a-e053-6394a90a16d6 |
| Associated GPIs | 72600075000310 |
| GCN Sequence Number | 029837 |
| GCN Sequence Number Description | topiramate TABLET 25 MG ORAL |
| HIC3 | H4B |
| HIC3 Description | ANTICONVULSANTS |
| GCN | 36553 |
| HICL Sequence Number | 011060 |
| HICL Sequence Number Description | TOPIRAMATE |
| Brand/Generic | Generic |
| Proprietary Name | TOPIRAMATE |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | TOPIRAMATE |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 25 |
| Active Ingredient Units | mg/1 |
| Substance Name | TOPIRAMATE |
| Labeler Name | Direct_Rx |
| Pharmaceutical Class | Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 3A4 Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA078235 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 61919-0883-30 (61919088330)
| NDC Package Code | 61919-883-30 |
|---|---|
| Billing NDC | 61919088330 |
| Package | 30 TABLET, FILM COATED in 1 BOTTLE (61919-883-30) |
| Marketing Start Date | 2019-05-31 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |