# Nabumetone

NDC: 70518-4047
Generic name: Nabumetone
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20240407

FDA application: ANDA078420

## Active ingredients

- NABUMETONE: 750 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-4047"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4047
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6106afa3-e138-4b4d-8c13-992bf5062097