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NDC 72237-101, selinexor, tablet, film coated, from Karyopharm Therapeutics Inc..

Product NDC
72237-101
Status
Listed
Labeler
Karyopharm Therapeutics Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA212306
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72237-101 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SELINEXOR20 mg/1

Pharmacologic classes

Nuclear Export Inhibitor [EPC]; Nuclear Export Inhibitors [MoA]

Package NDCNDC-11Package
72237-101-03722370101034 BLISTER PACK in 1 CARTON (72237-101-03) / 6 TABLET, FILM COATED in 1 BLISTER PACK (72237-101-13)
72237-101-04722370101044 BLISTER PACK in 1 CARTON (72237-101-04) / 8 TABLET, FILM COATED in 1 BLISTER PACK (72237-101-14)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f6dd2682-75a6-4863-90a8-a3197f6f78a8

Use it

Look up 72237-101 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72237-101 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72237-101. 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.