Back to search
🇺🇸

United States · US · US:72237-103_5e9b366c-3fc4-4178-bb80-687e21f9beff

XPOVIO

Orange BookUNIISPLATC L01XX66

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerKaryopharm Therapeutics Inc.
CountryUS (United States)
ATC codeL01XX66
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    7223710305
    4 BLISTER PACK in 1 CARTON (72237-103-05) / 2 TABLET, FILM COATED in 1 BLISTER PACK (72237-103-15)

Annotations

UNII (FDA Substance ID)
31TZ62FO8F
SELINEXOR
RxCUI 2178390
Orange Book
N212306
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "31TZ62FO8F",
    "rxcui": "2178390",
    "inchikey": "DEVSOMFAQLZNKR-RJRFIUFISA-N",
    "display_name": "SELINEXOR",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "f6dd2682-75a6-4863-90a8-a3197f6f78a8": {
      "match": "brand_token",
      "title": "XPOVIO (SELINEXOR) TABLET, FILM COATED [KARYOPHARM THERAPEUTICS INC.]",
      "spl_version": "18",
      "published_date": "2026-05-13"
    }
  },
  "productid": "72237-103_5e9b366c-3fc4-4178-bb80-687e21f9beff",
  "productndc": "72237-103",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "212306",
    "products": [
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "20MG",
        "product_no": "001",
        "approval_date": "Jul 3, 2019"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "40MG",
        "product_no": "002",
        "approval_date": "Apr 15, 2021"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "50MG",
        "product_no": "003",
        "approval_date": "Apr 15, 2021"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": null,
        "strength": "60MG",
        "product_no": "004",
        "approval_date": "Apr 15, 2021"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "10MG",
        "product_no": "005",
        "approval_date": "Mar 10, 2025"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "80MG",
        "product_no": "006",
        "approval_date": "Oct 20, 2025"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "SELINEXOR",
  "proprietary_name": "XPOVIO",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA212306",
  "marketing_category": "NDA",
  "nonproprietary_name": "selinexor",
  "start_marketing_date": "20210519",
  "active_numerator_strength": "50"
}

Related drugs

Other records sharing ATC code L01XX66.

Access this data programmatically

Query XPOVIO and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.