United States · FDA National Drug Code directory
Nitazoxanide
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
- 64980-526_9ee8087a-d001-42a9-ae98-6e4cbf93caa1
- Product NDC
- 64980-526
- Form
- TABLET, FILM COATED
- Composition / generic term
- Nitazoxanide
- Labeler
- Rising Pharma Holdings, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201127
- Source listing expiry
- 20261231
Source-listed ingredients
- NITAZOXANIDE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (64980-526-03) · 64980-526-03
- 12 TABLET, FILM COATED in 1 BOTTLE (64980-526-21) · 64980-526-21
- 6 TABLET, FILM COATED in 1 BOTTLE (64980-526-60) · 64980-526-60
- 18 TABLET, FILM COATED in 1 BOTTLE (64980-526-81) · 64980-526-81
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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