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
- 14445-172_7394738d-e6ca-4be9-9fb8-28702362abc5
- Product NDC
- 14445-172
- Form
- TABLET
- Composition / generic term
- Allopurinol
- Labeler
- Indoco Remedies Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240515
- Source listing expiry
- 20261231
Source-listed ingredients
- ALLOPURINOL — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE (14445-172-00) · 14445-172-00
- 100 TABLET in 1 BOTTLE (14445-172-01) · 14445-172-01
- 500 TABLET in 1 BOTTLE (14445-172-05) · 14445-172-05
- 10 BLISTER PACK in 1 CARTON (14445-172-10) / 10 TABLET in 1 BLISTER PACK (14445-172-02) · 14445-172-10
- 90 TABLET in 1 BOTTLE (14445-172-90) · 14445-172-90
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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