NDC 70518-1937 – Topiramate

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

Human Prescription Drug

Product NDC70518-1937

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078235
Marketed since
March 6, 2019
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (5)

Package NDCDescriptionSince
70518-1937-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-1937-0)Mar 6, 2019
70518-1937-3100 POUCH in 1 BOX (70518-1937-3) / 1 TABLET, FILM COATED in 1 POUCH (70518-1937-4)Jul 7, 2021
70518-1937-5120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1937-5)Apr 8, 2024
70518-1937-6180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1937-6)Jul 1, 2025
70518-1937-7120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1937-7)Mar 16, 2026

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