NDC 71335-0487 – Topiramate

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

Human Prescription Drug

Product NDC71335-0487

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090278
Marketed since
December 15, 2014
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0487-020 TABLET, FILM COATED in 1 BOTTLE (71335-0487-0)Apr 3, 2024
71335-0487-130 TABLET, FILM COATED in 1 BOTTLE (71335-0487-1)Dec 4, 2018
71335-0487-260 TABLET, FILM COATED in 1 BOTTLE (71335-0487-2)Dec 10, 2018
71335-0487-390 TABLET, FILM COATED in 1 BOTTLE (71335-0487-3)Apr 9, 2021
71335-0487-4120 TABLET, FILM COATED in 1 BOTTLE (71335-0487-4)May 5, 2021
71335-0487-57 TABLET, FILM COATED in 1 BOTTLE (71335-0487-5)Apr 3, 2024
71335-0487-680 TABLET, FILM COATED in 1 BOTTLE (71335-0487-6)Apr 3, 2024
71335-0487-714 TABLET, FILM COATED in 1 BOTTLE (71335-0487-7)Oct 10, 2022
71335-0487-845 TABLET, FILM COATED in 1 BOTTLE (71335-0487-8)Apr 3, 2024
71335-0487-928 TABLET, FILM COATED in 1 BOTTLE (71335-0487-9)Sep 15, 2021

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