# Nabumetone

NDC: 71335-1391
Generic name: Nabumetone
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190626

FDA application: ANDA078420

## Active ingredients

- NABUMETONE: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-1391"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-1391
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=62f2e0bf-e5c8-480c-ac5e-401ced3bbc67