NDC 71335-1684 – Topiramate

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

Human Prescription Drug

Product NDC71335-1684

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078235
Marketed since
March 27, 2009
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (10)

Package NDCDescriptionSince
71335-1684-028 TABLET, FILM COATED in 1 BOTTLE (71335-1684-0)Aug 14, 2020
71335-1684-130 TABLET, FILM COATED in 1 BOTTLE (71335-1684-1)Aug 7, 2020
71335-1684-260 TABLET, FILM COATED in 1 BOTTLE (71335-1684-2)Jul 31, 2020
71335-1684-390 TABLET, FILM COATED in 1 BOTTLE (71335-1684-3)Sep 30, 2020
71335-1684-456 TABLET, FILM COATED in 1 BOTTLE (71335-1684-4)May 20, 2024
71335-1684-584 TABLET, FILM COATED in 1 BOTTLE (71335-1684-5)Apr 29, 2022
71335-1684-6120 TABLET, FILM COATED in 1 BOTTLE (71335-1684-6)Sep 3, 2020
71335-1684-77 TABLET, FILM COATED in 1 BOTTLE (71335-1684-7)Mar 18, 2021
71335-1684-814 TABLET, FILM COATED in 1 BOTTLE (71335-1684-8)Sep 10, 2020
71335-1684-945 TABLET, FILM COATED in 1 BOTTLE (71335-1684-9)Apr 29, 2022

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