NDC 68788-7468 – Topiramate

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

Human Prescription Drug

Product NDC68788-7468

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078235
Marketed since
March 2, 2020
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (4)

Package NDCDescriptionSince
68788-7468-330 TABLET, FILM COATED in 1 BOTTLE (68788-7468-3)Mar 2, 2020
68788-7468-515 TABLET, FILM COATED in 1 BOTTLE (68788-7468-5)Mar 2, 2020
68788-7468-660 TABLET, FILM COATED in 1 BOTTLE (68788-7468-6)Mar 2, 2020
68788-7468-990 TABLET, FILM COATED in 1 BOTTLE (68788-7468-9)Mar 2, 2020

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