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
- 71335-0090_acf0fa26-5b16-424b-9e49-91ee29c7e5fd
- Product NDC
- 71335-0090
- Form
- TABLET, FILM COATED
- Composition / generic term
- OXCARBAZEPINE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20080111
- 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 (71335-0090-1) · 71335-0090-1
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-0090-2) · 71335-0090-2
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-0090-3) · 71335-0090-3
- 180 TABLET, FILM COATED in 1 BOTTLE (71335-0090-4) · 71335-0090-4
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-0090-5) · 71335-0090-5
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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