NDC 71335-1147 – Topiramate

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

Human Prescription Drug

Product NDC71335-1147

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
71335-1147-020 TABLET, FILM COATED in 1 BOTTLE (71335-1147-0)May 2, 2022
71335-1147-130 TABLET, FILM COATED in 1 BOTTLE (71335-1147-1)Mar 29, 2019
71335-1147-260 TABLET, FILM COATED in 1 BOTTLE (71335-1147-2)Mar 4, 2019
71335-1147-390 TABLET, FILM COATED in 1 BOTTLE (71335-1147-3)Mar 14, 2019
71335-1147-4120 TABLET, FILM COATED in 1 BOTTLE (71335-1147-4)Feb 4, 2020
71335-1147-57 TABLET, FILM COATED in 1 BOTTLE (71335-1147-5)Aug 3, 2020
71335-1147-680 TABLET, FILM COATED in 1 BOTTLE (71335-1147-6)May 2, 2022
71335-1147-714 TABLET, FILM COATED in 1 BOTTLE (71335-1147-7)Nov 2, 2020
71335-1147-845 TABLET, FILM COATED in 1 BOTTLE (71335-1147-8)May 2, 2022
71335-1147-928 TABLET, FILM COATED in 1 BOTTLE (71335-1147-9)Aug 14, 2020

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