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
- 71335-0925_01e04859-b5e0-4061-b270-c85cef0fe7e4
- Product NDC
- 71335-0925
- Form
- TABLET, FILM COATED
- Composition / generic term
- Topiramate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20141215
- Source listing expiry
- 20271231
Source-listed ingredients
- TOPIRAMATE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-0925-1) · 71335-0925-1
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-0925-2) · 71335-0925-2
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-0925-3) · 71335-0925-3
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-0925-4) · 71335-0925-4
- 28 TABLET, FILM COATED in 1 BOTTLE (71335-0925-5) · 71335-0925-5
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-0925-6) · 71335-0925-6
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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