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
- 55111-729_15f5d0a0-98ae-aa59-3a4d-d20efebbc6f6
- Product NDC
- 55111-729
- Form
- TABLET
- Composition / generic term
- allopurinol
- Labeler
- Dr. Reddy's Laboratories Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20091001
- Source listing expiry
- 20271231
Source-listed ingredients
- ALLOPURINOL — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (55111-729-01) · 55111-729-01
- 1000 TABLET in 1 BOTTLE (55111-729-10) · 55111-729-10
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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