NDC 67046-1691 – Topiramate

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

Human Prescription Drug

Product NDC67046-1691

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Coupler LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090162
Marketed since
August 3, 2026
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (1)

Package NDCDescriptionSince
67046-1691-330 TABLET, FILM COATED in 1 BLISTER PACK (67046-1691-3)Aug 3, 2026

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