# Nabumetone

NDC: 60687-630
Generic name: Nabumetone
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220323

FDA application: ANDA078671

## Active ingredients

- NABUMETONE: 500 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60687-630"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-630
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0653b873-b74b-4ec6-b112-675760703d91