NDC 80425-0092 – Topiramate

Topiramate 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC80425-0092

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Advanced Rx Pharmacy of Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078235
Marketed since
March 27, 2009
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (3)

Package NDCDescriptionSince
80425-0092-130 TABLET, FILM COATED in 1 BOTTLE (80425-0092-1)Mar 27, 2009
80425-0092-260 TABLET, FILM COATED in 1 BOTTLE (80425-0092-2)Mar 27, 2009
80425-0092-390 TABLET, FILM COATED in 1 BOTTLE (80425-0092-3)Aug 14, 2024

Other Topiramate products