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United States · US · US:73042-201_75b08b15-496c-4b4c-bf71-f0220b0d58b3
DANYELZA
UNIISPLATC L01FX21
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerY-mAbs Therapeutics, Inc.
CountryUS (United States)
ATC codeL01FX21
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1173042201011 VIAL, SINGLE-DOSE in 1 CARTON (73042-201-01) / 10 mL in 1 VIAL, SINGLE-DOSE
Annotations
UNII (FDA Substance ID)
9K8GNJ2874
NAXITAMAB
RxCUI 2474039
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "9K8GNJ2874",
"rxcui": "2474039",
"inchikey": null,
"display_name": "NAXITAMAB",
"substance_type": "protein",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"b0f5ee96-369f-4cb9-a783-3bfa70fe8f90": {
"match": "brand_token",
"title": "DANYELZA (NAXITAMAB) INJECTION [BTG INTERNATIONAL INC.]",
"spl_version": "2",
"published_date": "2026-06-01"
}
},
"productid": "73042-201_75b08b15-496c-4b4c-bf71-f0220b0d58b3",
"productndc": "73042-201",
"dosage_form": "INJECTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "NAXITAMAB",
"proprietary_name": "DANYELZA",
"active_ingred_unit": "mg/10mL",
"application_number": "BLA761171",
"marketing_category": "BLA",
"nonproprietary_name": "Naxitamab",
"start_marketing_date": "20201125",
"active_numerator_strength": "40"
}Related drugs
Other records sharing ATC code L01FX21.
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