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: 82638-113_2b4201b6-c125-05d2-e063-6294a90a58c1
Product NDC: 82638-113
Form: TABLET
Composition / generic term: Allopurinol
Labeler: Harman Finochem Limited
Marketing category: ANDA
Marketing start / end (source format): 20231006
Source listing expiry: 20261231

Source-listed ingredients

ALLOPURINOL — 300 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 TABLET in 1 BOTTLE (82638-113-02) · 82638-113-02
500 TABLET in 1 BOTTLE (82638-113-03) · 82638-113-03
1000 TABLET in 1 BOTTLE (82638-113-04) · 82638-113-04

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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