NDC 68788-8817 – Topiramate

Topiramate 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68788-8817

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 21, 2025
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (5)

Package NDCDescriptionSince
68788-8817-330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8817-3)Jan 21, 2025
68788-8817-515 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8817-5)Jan 21, 2025
68788-8817-660 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8817-6)Jan 21, 2025
68788-8817-8120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8817-8)Jan 21, 2025
68788-8817-990 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8817-9)Jan 21, 2025

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