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NDC 72237-102, selinexor, tablet, film coated, from Karyopharm Therapeutics Inc..

Product NDC
72237-102
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/72237-102 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SELINEXOR40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72237-102-02722370102024 BLISTER PACK in 1 CARTON (72237-102-02) / 2 TABLET, FILM COATED in 1 BLISTER PACK (72237-102-12)
72237-102-06722370102064 BLISTER PACK in 1 CARTON (72237-102-06) / 2 TABLET, FILM COATED in 1 BLISTER PACK (72237-102-16)
72237-102-07722370102074 BLISTER PACK in 1 CARTON (72237-102-07) / 1 TABLET, FILM COATED in 1 BLISTER PACK (72237-102-17)

Linked data

RxNorm, label and prices

Use it

Look up 72237-102 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72237-102 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72237-102. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.