NDC 70518-2001 – Topiramate

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

Human Prescription Drug

Product NDC70518-2001

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078235
Marketed since
April 3, 2019
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (3)

Package NDCDescriptionSince
70518-2001-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-2001-0)Apr 3, 2019
70518-2001-1100 POUCH in 1 BOX (70518-2001-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-2001-2)Dec 10, 2019
70518-2001-650 POUCH in 1 BOX (70518-2001-6) / 1 TABLET, FILM COATED in 1 POUCH (70518-2001-4)Jul 8, 2026

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