NDC 68788-4067 – Topiramate

Topiramate 200 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68788-4067

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090162
Marketed since
January 28, 2026
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (4)

Package NDCDescriptionSince
68788-4067-330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4067-3)Jan 28, 2026
68788-4067-515 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4067-5)Jan 28, 2026
68788-4067-660 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4067-6)Jan 28, 2026
68788-4067-990 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4067-9)Jan 28, 2026

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