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
- 71335-0487_ebf813da-167b-44ed-921d-015fdc8b6d61
- Product NDC
- 71335-0487
- Form
- TABLET, FILM COATED
- Composition / generic term
- Topiramate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20141215
- Source listing expiry
- 20261231
Source-listed ingredients
- TOPIRAMATE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-0487-0) · 71335-0487-0
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-0487-1) · 71335-0487-1
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-0487-2) · 71335-0487-2
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-0487-3) · 71335-0487-3
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-0487-4) · 71335-0487-4
- 7 TABLET, FILM COATED in 1 BOTTLE (71335-0487-5) · 71335-0487-5
- 80 TABLET, FILM COATED in 1 BOTTLE (71335-0487-6) · 71335-0487-6
- 14 TABLET, FILM COATED in 1 BOTTLE (71335-0487-7) · 71335-0487-7
- 45 TABLET, FILM COATED in 1 BOTTLE (71335-0487-8) · 71335-0487-8
- 28 TABLET, FILM COATED in 1 BOTTLE (71335-0487-9) · 71335-0487-9
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 →