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
33342-274_eb38172a-f884-4a94-be6d-73ad338fb29c
Product NDC
33342-274
Form
FILM
Composition / generic term
Febuxostat tablets 40 mg
Labeler
Macleods Pharmaceuticals Limited
Marketing category
ANDA
Marketing start / end (source format)
20190404
Source listing expiry
20261231

Source-listed ingredients

  • FEBUXOSTAT — 40 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 FILM in 1 BOTTLE (33342-274-07) · 33342-274-07
  • 90 FILM in 1 BOTTLE (33342-274-10) · 33342-274-10
  • 500 FILM in 1 BOTTLE (33342-274-15) · 33342-274-15

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 →