United States · FDA National Drug Code directory

Trileptal

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
0078-0457_dcd739ce-e938-40e6-8912-ca4f34b49cf3
Product NDC
0078-0457
Form
TABLET, FILM COATED
Composition / generic term
oxcarbazepine
Labeler
Novartis Pharmaceuticals Corporation
Marketing category
NDA
Marketing start / end (source format)
20000130
Source listing expiry
20261231

Source-listed ingredients

  • OXCARBAZEPINE — 600 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET, FILM COATED in 1 BOTTLE (0078-0457-05) · 0078-0457-05
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0078-0457-35) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0078-0457-61) · 0078-0457-35

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 →