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United States · US · US:47335-177_7718538c-3c74-4470-9951-cf9634ab2f31
ILUMYA
UNIISPLATC L04AC17
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSun Pharmaceutical Industries, Inc.
CountryUS (United States)
ATC codeL04AC17
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc1147335177011 mL in 1 SYRINGE, GLASS (47335-177-01)
- ndc1147335177101 mL in 1 CARTON (47335-177-10)
- ndc1147335177951 mL in 1 CARTON (47335-177-95)
- ndc1147335177961 mL in 1 SYRINGE, GLASS (47335-177-96)
Annotations
UNII (FDA Substance ID)
DEW6X41BEK
TILDRAKIZUMAB
RxCUI 2053436
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "DEW6X41BEK",
"rxcui": "2053436",
"inchikey": null,
"display_name": "TILDRAKIZUMAB",
"substance_type": "protein",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "SUBCUTANEOUS",
"spl_meta": {
"c6a322bb-51b9-4f0e-8642-62a9682ffcde": {
"match": "brand_token",
"title": "ILUMYA (TILDRAKIZUMAB-ASMN) INJECTION, SOLUTION [SUN PHARMACEUTICAL INDUSTRIES, INC.]",
"spl_version": "18",
"published_date": "2025-12-26"
}
},
"productid": "47335-177_7718538c-3c74-4470-9951-cf9634ab2f31",
"productndc": "47335-177",
"dosage_form": "INJECTION, SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "TILDRAKIZUMAB",
"proprietary_name": "ILUMYA",
"active_ingred_unit": "mg/mL",
"application_number": "BLA761067",
"marketing_category": "BLA",
"nonproprietary_name": "tildrakizumab-asmn",
"start_marketing_date": "20180806",
"active_numerator_strength": "100"
}Related drugs
Other records sharing ATC code L04AC17.
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