XPOVIO

Product NDC
72237-105
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
selinexor
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Karyopharm Therapeutics Inc.
Application
NDA212306
Marketing category
NDA
Substance
SELINEXOR
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72237-105-014 BLISTER PACK in 1 CARTON (72237-105-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (72237-105-11) 2026-01-05NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
XPOVIOKaryopharm Therapeutics Inc.2026-05-12HUMAN PRESCRIPTION DRUG LABEL18