# Oxcarbazepine

NDC: 60290-067
Generic name: Oxcarbazepine
Labeler / Manufacturer: Umedica Laboratories USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260101

FDA application: ANDA218341

## Active ingredients

- OXCARBAZEPINE: 150 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60290-067"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60290-067
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e46d4654-76bc-4c33-ac2b-e89ae11b7697