NDC 51655-032 Topiramate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51655 - Northwind Pharmaceuticals, Llc
- 51655-032 - Topiramate
Product Characteristics
Product Packages
NDC Code 51655-032-52
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING
Product Details
What is NDC 51655-032?
What are the uses for Topiramate?
Which are Topiramate UNII Codes?
The UNII codes for the active ingredients in this product are:
- TOPIRAMATE (UNII: 0H73WJJ391)
- TOPIRAMATE (UNII: 0H73WJJ391) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Topiramate?
- RxCUI: 199888 - topiramate 25 MG Oral Tablet
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Patient Education
Topiramate
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.
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".