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
- 71335-1234_8b05e389-e1cc-47d1-b24e-10f247ca7f14
- Product NDC
- 71335-1234
- Form
- TABLET, FILM COATED
- Composition / generic term
- Nabumetone
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110613
- Source listing expiry
- 20261231
Source-listed ingredients
- NABUMETONE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-1234-1) · 71335-1234-1
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-1234-2) · 71335-1234-2
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-1234-3) · 71335-1234-3
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-1234-4) · 71335-1234-4
- 42 TABLET, FILM COATED in 1 BOTTLE (71335-1234-5) · 71335-1234-5
- 56 TABLET, FILM COATED in 1 BOTTLE (71335-1234-6) · 71335-1234-6
- 14 TABLET, FILM COATED in 1 BOTTLE (71335-1234-7) · 71335-1234-7
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-1234-8) · 71335-1234-8
- 9 TABLET, FILM COATED in 1 BOTTLE (71335-1234-9) · 71335-1234-9
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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