NDC 71335-1116 – Topiramate

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

Human Prescription Drug

Product NDC71335-1116

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 (6)

Package NDCDescriptionSince
71335-1116-130 TABLET, FILM COATED in 1 BOTTLE (71335-1116-1)Oct 22, 2020
71335-1116-260 TABLET, FILM COATED in 1 BOTTLE (71335-1116-2)Feb 22, 2019
71335-1116-390 TABLET, FILM COATED in 1 BOTTLE (71335-1116-3)Jul 8, 2022
71335-1116-4120 TABLET, FILM COATED in 1 BOTTLE (71335-1116-4)Jul 8, 2022
71335-1116-528 TABLET, FILM COATED in 1 BOTTLE (71335-1116-5)Jul 8, 2022
71335-1116-620 TABLET, FILM COATED in 1 BOTTLE (71335-1116-6)Jul 8, 2022

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