NDC 71335-1064 – Topiramate

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

Human Prescription Drug

Product NDC71335-1064

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090162
Marketed since
July 1, 2013
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (10)

Package NDCDescriptionSince
71335-1064-020 TABLET, FILM COATED in 1 BOTTLE (71335-1064-0)Jan 23, 2019
71335-1064-130 TABLET, FILM COATED in 1 BOTTLE (71335-1064-1)Jan 23, 2019
71335-1064-260 TABLET, FILM COATED in 1 BOTTLE (71335-1064-2)Jan 11, 2019
71335-1064-390 TABLET, FILM COATED in 1 BOTTLE (71335-1064-3)Jan 15, 2019
71335-1064-4120 TABLET, FILM COATED in 1 BOTTLE (71335-1064-4)Jan 23, 2019
71335-1064-57 TABLET, FILM COATED in 1 BOTTLE (71335-1064-5)Jan 31, 2019
71335-1064-680 TABLET, FILM COATED in 1 BOTTLE (71335-1064-6)Jan 23, 2019
71335-1064-714 TABLET, FILM COATED in 1 BOTTLE (71335-1064-7)May 31, 2019
71335-1064-845 TABLET, FILM COATED in 1 BOTTLE (71335-1064-8)Jan 23, 2019
71335-1064-928 TABLET, FILM COATED in 1 BOTTLE (71335-1064-9)Jan 23, 2019

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