NDC 71335-0548 – Topiramate

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

Human Prescription Drug

Product NDC71335-0548

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
71335-0548-028 TABLET, FILM COATED in 1 BOTTLE (71335-0548-0)Sep 15, 2021
71335-0548-130 TABLET, FILM COATED in 1 BOTTLE (71335-0548-1)Mar 19, 2018
71335-0548-260 TABLET, FILM COATED in 1 BOTTLE (71335-0548-2)Mar 5, 2018
71335-0548-390 TABLET, FILM COATED in 1 BOTTLE (71335-0548-3)Feb 15, 2018
71335-0548-456 TABLET, FILM COATED in 1 BOTTLE (71335-0548-4)Apr 3, 2024
71335-0548-584 TABLET, FILM COATED in 1 BOTTLE (71335-0548-5)Apr 3, 2024
71335-0548-6120 TABLET, FILM COATED in 1 BOTTLE (71335-0548-6)Mar 1, 2018
71335-0548-77 TABLET, FILM COATED in 1 BOTTLE (71335-0548-7)Apr 23, 2018
71335-0548-814 TABLET, FILM COATED in 1 BOTTLE (71335-0548-8)Jan 23, 2019
71335-0548-945 TABLET, FILM COATED in 1 BOTTLE (71335-0548-9)Apr 3, 2024

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