United States · FDA National Drug Code directory
ALLOPURINOL
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
- 80425-0518_36c1d44f-f581-f2ef-e063-6294a90a9f43
- Product NDC
- 80425-0518
- Form
- TABLET
- Composition / generic term
- ALLOPURINOL
- Labeler
- Advanced Rx of Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250529
- Source listing expiry
- 20261231
Source-listed ingredients
- ALLOPURINOL — 300 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (80425-0518-1) · 80425-0518-1
- 60 TABLET in 1 BOTTLE (80425-0518-2) · 80425-0518-2
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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