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United States · US · US:25682-025_41262953-a849-4095-b9c2-5a1d8b0238cc
Ultomiris
UNIISPLATC L04AJ02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAlexion Pharmaceuticals Inc.
CountryUS (United States)
ATC codeL04AJ02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1125682025011 VIAL, GLASS in 1 CARTON (25682-025-01) / 3 mL in 1 VIAL, GLASS
Annotations
UNII (FDA Substance ID)
C3VX249T6L
RAVULIZUMAB
RxCUI 2107301
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "C3VX249T6L",
"rxcui": "2107301",
"inchikey": null,
"display_name": "RAVULIZUMAB",
"substance_type": "protein",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"a9a590d9-0217-43c7-908d-e62a71279791": {
"match": "brand_token",
"title": "ULTOMIRIS (RAVULIZUMAB) SOLUTION, CONCENTRATE [ALEXION PHARMACEUTICALS INC.]",
"spl_version": "19",
"published_date": "2025-11-17"
}
},
"productid": "25682-025_41262953-a849-4095-b9c2-5a1d8b0238cc",
"productndc": "25682-025",
"dosage_form": "SOLUTION, CONCENTRATE",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "RAVULIZUMAB",
"proprietary_name": "Ultomiris",
"active_ingred_unit": "mg/3mL",
"application_number": "BLA761108",
"marketing_category": "BLA",
"nonproprietary_name": "ravulizumab",
"start_marketing_date": "20201009",
"active_numerator_strength": "300"
}Related drugs
Other records sharing ATC code L04AJ02.
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