# Nabumetone

NDC: 63187-307
Generic name: Nabumetone
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20110613

FDA application: ANDA091083

## Active ingredients

- NABUMETONE: 750 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63187-307"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63187-307
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=079a8a9e-6d71-414a-83f3-ef68e323c1fd