NDC 50090-5853 – Topiramate

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

Human Prescription Drug

Product NDC50090-5853

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078235
Marketed since
March 27, 2009
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (3)

Package NDCDescriptionSince
50090-5853-060 TABLET, FILM COATED in 1 BOTTLE (50090-5853-0)Nov 10, 2021
50090-5853-190 TABLET, FILM COATED in 1 BOTTLE (50090-5853-1)Nov 10, 2021
50090-5853-230 TABLET, FILM COATED in 1 BOTTLE (50090-5853-2)Nov 10, 2021

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