NDC 68071-4877 – Topiramate

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

Human Prescription Drug

Product NDC68071-4877

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
NuCare Pharmaceuticals,Inc.
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 (1)

Package NDCDescriptionSince
68071-4877-330 TABLET, FILM COATED in 1 BOTTLE (68071-4877-3)May 1, 2019

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