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NDC 59572-730, azacitidine, tablet, film coated, from Celgene Corporation.

Product NDC
59572-730
Status
Listed
Labeler
Celgene Corporation
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA214120
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59572-730 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AZACITIDINE200 mg/1

Pharmacologic classes

Nucleic Acid Synthesis Inhibitors [MoA]; Nucleoside Metabolic Inhibitor [EPC]

Package NDCNDC-11Package
59572-730-07595720730077 TABLET, FILM COATED in 1 BLISTER PACK (59572-730-07)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0e95e33f-8aba-4f19-b332-2416580d358b

Use it

Look up 59572-730 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59572-730 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59572-730. 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.