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
72162-1149_90912dd4-5abf-4fd3-8fc1-3afd057b743f
Product NDC
72162-1149
Form
TABLET
Composition / generic term
allopurinol
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20030627
Source listing expiry
20261231

Source-listed ingredients

  • ALLOPURINOL — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1000 TABLET in 1 BOTTLE (72162-1149-0) · 72162-1149-0

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 →