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
0615-8635_ad0a4e51-2bd3-4291-88bd-804083ae618b
Product NDC
0615-8635
Form
TABLET, FILM COATED
Composition / generic term
Oxcarbazepine
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Marketing category
ANDA
Marketing start / end (source format)
20250715
Source listing expiry
20271231

Source-listed ingredients

  • OXCARBAZEPINE — 300 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8635-39) · 0615-8635-39

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.

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Oxcarbazepine — United States | Molindra Medicines