United States · FDA National Drug Code directory
Revuforj
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
- 73555-501_76183831-b710-4be2-a6a7-9349dd501830
- Product NDC
- 73555-501
- Form
- TABLET, FILM COATED
- Composition / generic term
- revumenib
- Labeler
- Syndax Pharmaceuticals, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20241115
- Source listing expiry
- 20271231
Source-listed ingredients
- REVUMENIB CITRATE — 110 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73555-501-00) · 73555-501-00
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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