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United States · US · US:73604-914_11e22c54-9b9a-4f9f-8680-cb7327511a23
Arcalyst
UNIISPLATC L04AC04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerKiniksa Pharmaceuticals (UK), Ltd.
CountryUS (United States)
ATC codeL04AC04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1173604914011 VIAL, SINGLE-USE in 1 CARTON (73604-914-01) / 2 mL in 1 VIAL, SINGLE-USE
- ndc1173604914044 VIAL, SINGLE-USE in 1 CARTON (73604-914-04) / 2 mL in 1 VIAL, SINGLE-USE
Annotations
UNII (FDA Substance ID)
8K80YB5GMG
RILONACEPT
RxCUI 763450
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "8K80YB5GMG",
"rxcui": "763450",
"inchikey": null,
"display_name": "RILONACEPT",
"substance_type": "protein",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "SUBCUTANEOUS",
"spl_meta": {
"ad965f38-dd22-4607-a673-2fb92f3b527a": {
"match": "brand_token",
"title": "ARCALYST (RILONACEPT) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [KINIKSA PHARMACEUTICALS (UK), LTD.]",
"spl_version": "16",
"published_date": "2025-12-17"
}
},
"productid": "73604-914_11e22c54-9b9a-4f9f-8680-cb7327511a23",
"productndc": "73604-914",
"dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "RILONACEPT",
"proprietary_name": "Arcalyst",
"active_ingred_unit": "mg/2mL",
"application_number": "BLA125249",
"marketing_category": "BLA",
"nonproprietary_name": "rilonacept",
"start_marketing_date": "20080227",
"active_numerator_strength": "160"
}Related drugs
Other records sharing ATC code L04AC04.
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