United States · FDA National Drug Code directory
ULORIC
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
- 64764-677_16c36a5a-2f72-4df7-aa6f-1ca27a39404f
- Product NDC
- 64764-677
- Form
- TABLET
- Composition / generic term
- febuxostat
- Labeler
- Takeda Pharmaceuticals America, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20090213
- Source listing expiry
- 20261231
Source-listed ingredients
- FEBUXOSTAT — 80 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BLISTER PACK in 1 CARTON (64764-677-11) / 10 TABLET in 1 BLISTER PACK · 64764-677-11
- 100 TABLET in 1 BOTTLE (64764-677-13) · 64764-677-13
- 1000 TABLET in 1 BOTTLE (64764-677-19) · 64764-677-19
- 30 TABLET in 1 BOTTLE (64764-677-30) · 64764-677-30
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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