NDC 51655-608 – Topiramate

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

Human Prescription Drug

Product NDC51655-608

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077627
Marketed since
February 2, 2015
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (2)

Package NDCDescriptionSince
51655-608-2690 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (51655-608-26)Feb 2, 2015
51655-608-5230 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (51655-608-52)Feb 2, 2015

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