NDC 71205-214 – Topiramate

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

Human Prescription Drug

Product NDC71205-214

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090278
Marketed since
December 15, 2014
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (3)

Package NDCDescriptionSince
71205-214-3030 TABLET, FILM COATED in 1 BOTTLE (71205-214-30)Feb 1, 2019
71205-214-6060 TABLET, FILM COATED in 1 BOTTLE (71205-214-60)Feb 1, 2019
71205-214-9090 TABLET, FILM COATED in 1 BOTTLE (71205-214-90)Feb 1, 2019

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