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United States · US · US:73090-421_c32bb83e-f9f4-4a6e-928a-f736138996b6
Sylvant
UNIISPLATC L04AC11
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRecordati Rare Diseases, Inc.
CountryUS (United States)
ATC codeL04AC11
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1173090421011 VIAL, SINGLE-DOSE in 1 BOX (73090-421-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
Annotations
UNII (FDA Substance ID)
T4H8FMA7IM
SILTUXIMAB
RxCUI 1535218
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "T4H8FMA7IM",
"rxcui": "1535218",
"inchikey": null,
"display_name": "SILTUXIMAB",
"substance_type": "protein",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"8d663642-f52e-49c0-a023-2da083fdfc0b": {
"match": "brand_token",
"title": "SYLVANT (SILTUXIMAB) INJECTION, POWDER, FOR SOLUTION [RECORDATI RARE DISEASES, INC.]",
"spl_version": "7",
"published_date": "2024-08-29"
}
},
"productid": "73090-421_c32bb83e-f9f4-4a6e-928a-f736138996b6",
"productndc": "73090-421",
"dosage_form": "INJECTION, POWDER, FOR SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "SILTUXIMAB",
"proprietary_name": "Sylvant",
"active_ingred_unit": "mg/1",
"application_number": "BLA125496",
"marketing_category": "BLA",
"nonproprietary_name": "Siltuximab",
"start_marketing_date": "20140423",
"active_numerator_strength": "400"
}Related drugs
Other records sharing ATC code L04AC11.
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