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NDC 71335-0337-02 Topiramate 100 mg/1 Details

Topiramate 100 mg/1

Topiramate is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. 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: 71335-0337-02
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Topiramate

Product Information

NDC	71335-0337
Product ID	71335-0337_b224154a-6d3a-4a67-9939-bda44f9fdb87
Associated GPIs	72600075000330
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Topiramate
Proprietary Name Suffix	n/a
Non-Proprietary Name	Topiramate
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	100
Active Ingredient Units	mg/1
Substance Name	TOPIRAMATE
Labeler Name	Bryant Ranch Prepack
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	ANDA076343
Listing Certified Through	2024-12-31

Package

NDC 71335-0337-02 (71335033702)

Pricing Information	N/A
NDC Package Code	71335-0337-2
Billing NDC	71335033702
Package	30 TABLET in 1 BOTTLE (71335-0337-2)
Marketing Start Date	2022-02-09
NDC Exclude Flag	N