NDC 72162-2483 – Topiramate

Topiramate 200 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72162-2483

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090162
Marketed since
July 1, 2013
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (3)

Package NDCDescriptionSince
72162-2483-01000 TABLET, FILM COATED in 1 BOTTLE (72162-2483-0)May 1, 2025
72162-2483-5500 TABLET, FILM COATED in 1 BOTTLE (72162-2483-5)May 1, 2025
72162-2483-660 TABLET, FILM COATED in 1 BOTTLE (72162-2483-6)May 1, 2025

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