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
- 87063-208_52252957-7c1f-f080-e063-6394a90ac890
- Product NDC
- 87063-208
- Form
- TABLET, FILM COATED
- Composition / generic term
- Oxcarbazepine
- Labeler
- ASCLEMED USA INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220111
- Source listing expiry
- 20271231
Source-listed ingredients
- OXCARBAZEPINE — 300 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (87063-208-01) · 87063-208-01
- 30 TABLET, FILM COATED in 1 BOTTLE (87063-208-30) · 87063-208-30
- 60 TABLET, FILM COATED in 1 BOTTLE (87063-208-60) · 87063-208-60
- 90 TABLET, FILM COATED in 1 BOTTLE (87063-208-90) · 87063-208-90
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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