United States · FDA National Drug Code directory
Febuxostat
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
- 33342-275_eb38172a-f884-4a94-be6d-73ad338fb29c
- Product NDC
- 33342-275
- Form
- FILM
- Composition / generic term
- Febuxostat tablets 80 mg
- Labeler
- Macleods Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190404
- Source listing expiry
- 20261231
Source-listed ingredients
- FEBUXOSTAT — 80 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 FILM in 1 BOTTLE (33342-275-07) · 33342-275-07
- 90 FILM in 1 BOTTLE (33342-275-10) · 33342-275-10
- 500 FILM in 1 BOTTLE (33342-275-15) · 33342-275-15
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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