NDC 80425-0576 – Topiramate

Topiramate 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC80425-0576

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090162
Marketed since
February 18, 2026
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (4)

Package NDCDescriptionSince
80425-0576-130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0576-1)Feb 18, 2026
80425-0576-260 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0576-2)Feb 18, 2026
80425-0576-390 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0576-3)Feb 18, 2026
80425-0576-4270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0576-4)Feb 18, 2026

Other Topiramate products