NDC 51655-848 – Topiramate

Topiramate 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC51655-848

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
February 6, 2023
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (2)

Package NDCDescriptionSince
51655-848-2690 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-848-26)Apr 17, 2023
51655-848-5230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-848-52)Feb 6, 2023

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