# Nabumetone

NDC: 43063-972
Generic name: Nabumetone
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20190306

FDA application: ANDA078671

## Active ingredients

- NABUMETONE: 500 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43063-972"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43063-972
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8f3c1b1d-2765-4cb5-92df-044b99339c92