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
- 62756-711_b8c52970-05b0-43ea-9122-566998bf4524
- Product NDC
- 62756-711
- Form
- TABLET, FILM COATED
- Composition / generic term
- Topiramate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- 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
- 100 TABLET, FILM COATED in 1 BOTTLE (62756-711-08) · 62756-711-08
- 500 TABLET, FILM COATED in 1 BOTTLE (62756-711-13) · 62756-711-13
- 1000 TABLET, FILM COATED in 1 BOTTLE (62756-711-18) · 62756-711-18
- 30 TABLET, FILM COATED in 1 BOTTLE (62756-711-83) · 62756-711-83
- 60 TABLET, FILM COATED in 1 BOTTLE (62756-711-86) · 62756-711-86
- 100 TABLET, FILM COATED in 1 BOTTLE (62756-711-88) · 62756-711-88
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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