NDC 50090-2203 – Topiramate

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

Human Prescription Drug

Product NDC50090-2203

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
A-S Medication Solutions
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 (4)

Package NDCDescriptionSince
50090-2203-060 TABLET, FILM COATED in 1 BOTTLE (50090-2203-0)Oct 29, 2015
50090-2203-190 TABLET, FILM COATED in 1 BOTTLE (50090-2203-1)Oct 29, 2015
50090-2203-2120 TABLET, FILM COATED in 1 BOTTLE (50090-2203-2)Oct 29, 2015
50090-2203-3180 TABLET, FILM COATED in 1 BOTTLE (50090-2203-3)Feb 2, 2024

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