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
- 71335-0047_0fe6c993-9e52-4717-ad3e-d3999f42bfbd
- Product NDC
- 71335-0047
- Form
- TABLET
- Composition / generic term
- Topiramate
- Labeler
- Bryant Ranch Prepack
- 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 (71335-0047-1) · 71335-0047-1
- 60 TABLET in 1 BOTTLE (71335-0047-2) · 71335-0047-2
- 90 TABLET in 1 BOTTLE (71335-0047-3) · 71335-0047-3
- 120 TABLET in 1 BOTTLE (71335-0047-4) · 71335-0047-4
- 28 TABLET in 1 BOTTLE (71335-0047-5) · 71335-0047-5
- 20 TABLET in 1 BOTTLE (71335-0047-6) · 71335-0047-6
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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