# Trileptal

NDC: 0078-0457
Generic name: oxcarbazepine
Labeler / Manufacturer: Novartis Pharmaceuticals Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20000130

FDA application: NDA021014

## Active ingredients

- OXCARBAZEPINE: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0078-0457"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0078-0457
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4c5c86c8-ab7f-4fcf-bc1b-5a0b1fd0691b