NDC 68788-7351 – Topiramate

Topiramate 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68788-7351

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
February 27, 2019
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (5)

Package NDCDescriptionSince
68788-7351-1100 TABLET, FILM COATED in 1 BOTTLE (68788-7351-1)Feb 27, 2019
68788-7351-330 TABLET, FILM COATED in 1 BOTTLE (68788-7351-3)Feb 27, 2019
68788-7351-515 TABLET, FILM COATED in 1 BOTTLE (68788-7351-5)Feb 27, 2019
68788-7351-660 TABLET, FILM COATED in 1 BOTTLE (68788-7351-6)Feb 27, 2019
68788-7351-990 TABLET, FILM COATED in 1 BOTTLE (68788-7351-9)Feb 27, 2019

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