United States · FDA National Drug Code directory
Oxcarbazepine
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
- 71335-2548_99a631d2-4db5-4d59-9d54-a6334d7b9fac
- Product NDC
- 71335-2548
- Form
- TABLET, FILM COATED
- Composition / generic term
- Oxcarbazepine
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220111
- Source listing expiry
- 20261231
Source-listed ingredients
- OXCARBAZEPINE — 300 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-2548-1) · 71335-2548-1
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-2548-2) · 71335-2548-2
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-2548-3) · 71335-2548-3
- 180 TABLET, FILM COATED in 1 BOTTLE (71335-2548-4) · 71335-2548-4
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-2548-5) · 71335-2548-5
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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