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
- 71335-1391_6a56d60f-97bc-4895-9921-5141c7d03a5e
- Product NDC
- 71335-1391
- Form
- TABLET
- Composition / generic term
- Nabumetone
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190626
- Source listing expiry
- 20261231
Source-listed ingredients
- NABUMETONE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET in 1 BOTTLE (71335-1391-1) · 71335-1391-1
- 30 TABLET in 1 BOTTLE (71335-1391-2) · 71335-1391-2
- 60 TABLET in 1 BOTTLE (71335-1391-3) · 71335-1391-3
- 90 TABLET in 1 BOTTLE (71335-1391-4) · 71335-1391-4
- 42 TABLET in 1 BOTTLE (71335-1391-5) · 71335-1391-5
- 56 TABLET in 1 BOTTLE (71335-1391-6) · 71335-1391-6
- 14 TABLET in 1 BOTTLE (71335-1391-7) · 71335-1391-7
- 100 TABLET in 1 BOTTLE (71335-1391-8) · 71335-1391-8
- 9 TABLET in 1 BOTTLE (71335-1391-9) · 71335-1391-9
Source and coverage
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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.
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