NDC 72237-104

XPOVIO

Selinexor

XPOVIO is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Karyopharm Therapeutics Inc.. The primary component is Selinexor.

Product ID72237-104_0aa4ad93-ecc2-41b6-9668-ad45f3f32c61
NDC72237-104
Product TypeHuman Prescription Drug
Proprietary NameXPOVIO
Generic NameSelinexor
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2021-05-19
Marketing CategoryNDA /
Application NumberNDA212306
Labeler NameKaryopharm Therapeutics Inc.
Substance NameSELINEXOR
Active Ingredient Strength60 mg/1
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 72237-104-01

4 BLISTER PACK in 1 CARTON (72237-104-01) > 1 TABLET, FILM COATED in 1 BLISTER PACK (72237-104-11)
Marketing Start Date2021-05-19
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "XPOVIO" or generic name "Selinexor"

NDCBrand NameGeneric Name
72237-101XPOVIOselinexor
72237-102XPOVIOselinexor
72237-103XPOVIOselinexor
72237-104XPOVIOselinexor

Trademark Results [XPOVIO]

Mark Image

Registration | Serial
Company
Trademark
Application Date
XPOVIO
XPOVIO
87719728 not registered Live/Pending
Karyopharm Therapeutics Inc.
2017-12-13
XPOVIO
XPOVIO
86418181 not registered Dead/Abandoned
Karyopharm Therapeutics Inc.
2014-10-08

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.