NDC 51655-746 – Topiramate

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

Human Prescription Drug

Product NDC51655-746

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078235
Marketed since
December 30, 2022
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (2)

Package NDCDescriptionSince
51655-746-2690 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-746-26)Jan 5, 2023
51655-746-5230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-746-52)Dec 30, 2022

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