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
76420-280_e838b0d0-6869-8c20-e053-2a95a90a4d11
Product NDC
76420-280
Form
TABLET
Composition / generic term
Topiramate
Labeler
Asclemed USA, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20140612
Source listing expiry
20261231

Source-listed ingredients

  • TOPIRAMATE — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (76420-280-30) · 76420-280-30
  • 60 TABLET in 1 BOTTLE (76420-280-60) · 76420-280-60
  • 90 TABLET in 1 BOTTLE (76420-280-90) · 76420-280-90

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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