# Nabumetone

NDC: 50090-6167
Generic name: Nabumetone
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190626

FDA application: ANDA078420

## Active ingredients

- NABUMETONE: 750 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-6167"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-6167
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d997d125-dfc5-4cc5-b7a6-03f5a7248d14