XPOVIO
- Product NDC
- 72237-106
- 11-digit product format
- 722370106
- Labeler code
- 72237
- Product ID
- 72237-106_5e9b366c-3fc4-4178-bb80-687e21f9beff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- selinexor
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Karyopharm Therapeutics Inc.
- Application
- NDA212306
- Marketing category
- NDA
- Marketing start
- 2025-03-10
- Substance
- SELINEXOR
- Active strength
- 10 mg/1
- Pharmacologic classes
- Nuclear Export Inhibitor [EPC], Nuclear Export Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 31TZ62FO8F | SELINEXOR | 1393477-72-9 | SELINEXOR |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72237-106-01 | 72237010601 | 4 BLISTER PACK in 1 CARTON (72237-106-01) / 4 TABLET, FILM COATED in 1 BLISTER PACK (72237-106-11) | 4 blister pack | 2025-03-10 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| XPOVIO | Karyopharm Therapeutics Inc. | 2026-05-12 | HUMAN PRESCRIPTION DRUG LABEL | 18 |