NDC 0615-8593 – Topiramate

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

Human Prescription Drug

Product NDC0615-8593

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078462
Marketed since
March 27, 2009
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (1)

Package NDCDescriptionSince
0615-8593-3930 TABLET, FILM COATED in 1 BLISTER PACK (0615-8593-39)Oct 21, 2025

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