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United States · US · US:0299-6220_df0e2be2-b6bd-40e5-9175-0c8e893433ea
NEMLUVIO
UNIISPLATC D11AH12
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerGalderma Laboratories, L.P.
CountryUS (United States)
ATC codeD11AH12
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1102996220101 SYRINGE, GLASS in 1 CARTON (0299-6220-10) / 30 mg in 1 SYRINGE, GLASS
- ndc1102996220151 SYRINGE in 1 CARTON (0299-6220-15) / 30 mg in 1 SYRINGE
Annotations
UNII (FDA Substance ID)
GN465U8B72
NEMOLIZUMAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "GN465U8B72",
"rxcui": null,
"inchikey": null,
"display_name": "NEMOLIZUMAB",
"substance_type": "protein",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "SUBCUTANEOUS",
"spl_meta": {
"e9229ef1-ac60-4c24-afb6-009d3c781687": {
"match": "brand_token",
"title": "NEMLUVIO (NEMOLIZUMAB-ILTO) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [GALDERMA LABORATORIES, L.P.]",
"spl_version": "5",
"published_date": "2025-12-16"
}
},
"productid": "0299-6220_df0e2be2-b6bd-40e5-9175-0c8e893433ea",
"productndc": "0299-6220",
"dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "NEMOLIZUMAB",
"proprietary_name": "NEMLUVIO",
"active_ingred_unit": "mg/100mg",
"application_number": "BLA761390",
"marketing_category": "BLA",
"nonproprietary_name": "nemolizumab-ilto",
"start_marketing_date": "20240813",
"active_numerator_strength": "30"
}Related drugs
Other records sharing ATC code D11AH12.
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