# Nabumetone

NDC: 80425-0053
Generic name: Nabumetone
Labeler / Manufacturer: Advanced Rx of Tennessee, LLC
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

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80425-0053"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0053
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=af9969df-ce14-c0bc-e053-2995a90a3f59