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
68462-374_4a2276a1-54f6-4de6-8710-c2c088a23e76
Product NDC
68462-374
Form
CAPSULE, EXTENDED RELEASE
Composition / generic term
topiramate
Labeler
Glenmark Pharmaceuticals Inc., USA
Marketing category
ANDA
Marketing start / end (source format)
20210201
Source listing expiry
20271231

Source-listed ingredients

  • TOPIRAMATE — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-374-05) · 68462-374-05
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-374-30) · 68462-374-30
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-374-90) · 68462-374-90

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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