# Nabumetone

NDC: 70954-784
Generic name: Nabumetone
Labeler / Manufacturer: ANI Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250107

FDA application: ANDA219118

## Active ingredients

- NABUMETONE: 500 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70954-784"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70954-784
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e87289f4-d4f9-4510-aaa5-51f8f8167658