United States · FDA National Drug Code directory

TOPIRAMATE

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
63187-060_f68b2272-7a9d-4838-89ff-a10064e49015
Product NDC
63187-060
Form
TABLET, FILM COATED
Composition / generic term
TOPIRAMATE
Labeler
Proficient Rx LP
Marketing category
ANDA
Marketing start / end (source format)
20090327
Source listing expiry
20261231

Source-listed ingredients

  • TOPIRAMATE — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, FILM COATED in 1 BOTTLE (63187-060-30) · 63187-060-30

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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