# Oxcarbazepine

NDC: 68999-841
Generic name: Oxcarbazepine
Labeler / Manufacturer: Chartwell Governmental & Specialty RX, LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20210921

FDA application: ANDA212428

## Active ingredients

- OXCARBAZEPINE: 300 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68999-841"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68999-841
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e74bb389-8426-4ffc-a14b-a5990de6d0d4