NDC 71335-0047 – Topiramate

Topiramate 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0047

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076343
Marketed since
June 12, 2014
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (6)

Package NDCDescriptionSince
71335-0047-130 TABLET in 1 BOTTLE (71335-0047-1)May 4, 2018
71335-0047-260 TABLET in 1 BOTTLE (71335-0047-2)May 4, 2018
71335-0047-390 TABLET in 1 BOTTLE (71335-0047-3)May 4, 2018
71335-0047-4120 TABLET in 1 BOTTLE (71335-0047-4)May 4, 2018
71335-0047-528 TABLET in 1 BOTTLE (71335-0047-5)May 4, 2018
71335-0047-620 TABLET in 1 BOTTLE (71335-0047-6)May 4, 2018

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