United States · FDA National Drug Code directory
NABUMETONE
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 72189-072_2be95f19-e557-ab96-e063-6394a90a6947
- Product NDC
- 72189-072
- Form
- TABLET
- Composition / generic term
- NABUMETONE
- Labeler
- direct rx
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200618
- Source listing expiry
- 20261231
Source-listed ingredients
- NABUMETONE — 750 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 14 TABLET in 1 BOTTLE (72189-072-14) · 72189-072-14
- 30 TABLET in 1 BOTTLE (72189-072-30) · 72189-072-30
- 60 TABLET in 1 BOTTLE (72189-072-60) · 72189-072-60
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →