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United States · US · US:50881-033_baf91401-9bd0-4ce6-a5c4-7ca5c572f106
JAKAFI XR
UNIISPLATC D11AH09
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerIncyte Corporation
CountryUS (United States)
ATC codeD11AH09
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11508810330830 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50881-033-08)
Annotations
UNII (FDA Substance ID)
82S8X8XX8H
RUXOLITINIB
RxCUI 1193326
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "82S8X8XX8H",
"rxcui": "1193326",
"inchikey": "HFNKQEVNSGCOJV-OAHLLOKOSA-N",
"display_name": "RUXOLITINIB",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"f1c82580-87ae-11e0-bc84-0002a5d5c51b": {
"match": "brand_token",
"title": "JAKAFI (RUXOLITINIB) TABLET JAKAFI XR (RUXOLITINIB) TABLET, EXTENDED RELEASE [INCYTE CORPORATION]",
"spl_version": "40",
"published_date": "2026-05-11"
}
},
"productid": "50881-033_baf91401-9bd0-4ce6-a5c4-7ca5c572f106",
"productndc": "50881-033",
"dosage_form": "TABLET, EXTENDED RELEASE",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "RUXOLITINIB",
"proprietary_name": "JAKAFI XR",
"active_ingred_unit": "mg/1",
"application_number": "NDA217180",
"marketing_category": "NDA",
"nonproprietary_name": "ruxolitinib",
"start_marketing_date": "20260501",
"active_numerator_strength": "33"
}Related drugs
Other records sharing ATC code D11AH09.
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