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
71610-493_875c3303-147e-4bdf-98f2-8355c056e18f
Product NDC
71610-493
Form
TABLET
Composition / generic term
Topiramate
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Marketing category
ANDA
Marketing start / end (source format)
20200907
Source listing expiry
20261231

Source-listed ingredients

  • TOPIRAMATE — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 15 TABLET in 1 BOTTLE (71610-493-15) · 71610-493-15
  • 30 TABLET in 1 BOTTLE (71610-493-30) · 71610-493-30
  • 90 TABLET in 1 BOTTLE (71610-493-60) · 71610-493-60

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →