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
67296-1897_2c630c05-3e4e-fe4c-e063-6394a90a07cd
Product NDC
67296-1897
Form
TABLET
Composition / generic term
Allopurinol
Labeler
Redpharm Drug
Marketing category
ANDA
Marketing start / end (source format)
20200922
Source listing expiry
20261231

Source-listed ingredients

  • ALLOPURINOL — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (67296-1897-3) · 67296-1897-3

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 →