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
67544-736_887b4ea6-3af9-4825-b453-176d44169b86
Product NDC
67544-736
Form
TABLET
Composition / generic term
allopurinol
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Marketing category
ANDA
Marketing start / end (source format)
19861024
Source listing expiry
20261231

Source-listed ingredients

  • ALLOPURINOL — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET in 1 BOTTLE (67544-736-60) · 67544-736-60
  • 180 TABLET in 1 BOTTLE (67544-736-80) · 67544-736-80

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.

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Allopurinol — United States | Molindra Medicines