# Nabumetone

NDC: 76282-258
Generic name: Nabumetone
Labeler / Manufacturer: Exelan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20150414

FDA application: ANDA078671

## Active ingredients

- NABUMETONE: 750 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76282-258"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76282-258
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=16e76e29-9315-40c0-b1d6-8d91961063cf