NDC 62756-710 – Topiramate

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

Human Prescription Drug

Product NDC62756-710

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090278
Marketed since
March 27, 2009
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (6)

Package NDCDescriptionSince
62756-710-08100 TABLET, FILM COATED in 1 BOTTLE (62756-710-08)Mar 27, 2009
62756-710-13500 TABLET, FILM COATED in 1 BOTTLE (62756-710-13)Mar 27, 2009
62756-710-181000 TABLET, FILM COATED in 1 BOTTLE (62756-710-18)Mar 27, 2009
62756-710-8330 TABLET, FILM COATED in 1 BOTTLE (62756-710-83)Mar 27, 2009
62756-710-8660 TABLET, FILM COATED in 1 BOTTLE (62756-710-86)Mar 27, 2009
62756-710-88100 TABLET, FILM COATED in 1 BOTTLE (62756-710-88)Mar 27, 2009

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