Topiramate how supplied storage and handling

Topiramate
TOPIRAMATE® FDA Package Insert
Indications and Usage
Dosage and Administration
Dosage Forms and Strengths
Contraindications
Warnings and Precautions
Adverse Reactions
Drug Interactions
Use in Specific Populations
Overdosage
Description
Clinical Pharmacology
Nonclinical Toxicology
Clinical Studies
How Supplied/Storage and Handling
Patient Counseling Information
Labels and Packages
Clinical Trials on Topiramate
ClinicalTrials.gov

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Pratik Bahekar, MBBS [2]

For patient information about topiramate, click here.

How Supplied Storage and Handling

Topiramate Tablets USP

Topiramate Tablets USP, 25 mg are white, circular, biconvex, film-coated tablets debossed with ‘E’ on one side and ‘22’ on the other side.

     Bottles of 60                   NDC 65862-171-60

Topiramate Tablets USP, 50 mg are light yellow colored, circular, biconvex, film-coated tablets debossed with ‘E’ on one side and ‘33’ on the other side.

     Bottles of 60                   NDC 65862-172-60

Topiramate Tablets USP, 100 mg are dark yellow colored, circular, biconvex, beveled edge, film-coated tablets debossed with ‘E’ on one side and ‘23’ on the other side.

     Bottles of 60                   NDC 65862-173-60

Topiramate Tablets USP, 200 mg are pink colored, circular, biconvex, beveled edge, film-coated tablets debossed with ‘E’ on one side and ‘24’ on the other side.

     Bottles of 60                   NDC 65862-174-60

Storage and Handling

Store topiramate tablets in tightly-closed containers at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. Protect from moisture.