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Revuforj

NDC 73555-501, revumenib, tablet, film coated, from Syndax Pharmaceuticals, Inc..

Product NDC
73555-501
Status
Listed
Labeler
Syndax Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA218944
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/73555-501 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • REVUMENIB CITRATE110 mg/1

Pharmacologic classes

Menin Inhibitor [EPC]; Menin Inhibitors [MoA]

Package NDCNDC-11Package
73555-501-007355505010030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73555-501-00)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6eb3cdbc-0e74-477d-82d6-3bb172d3f63f

Use it

Look up 73555-501 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/73555-501 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 73555-501. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.