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United States · US · US:0078-0827_8b8e71f4-7d7e-40b5-a942-89ac3b6c0c6c
BEOVU
UNIISPLATC S01LA06
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNovartis Pharmaceuticals Corporation
CountryUS (United States)
ATC codeS01LA06
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1100780827601 SYRINGE, GLASS in 1 CARTON (0078-0827-60) / .05 mL in 1 SYRINGE, GLASS
- ndc1100780827981 SYRINGE, GLASS in 1 CARTON (0078-0827-98) / .05 mL in 1 SYRINGE, GLASS
Annotations
UNII (FDA Substance ID)
XSZ53G39H5
BROLUCIZUMAB
RxCUI 2204915
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "XSZ53G39H5",
"rxcui": "2204915",
"inchikey": null,
"display_name": "BROLUCIZUMAB",
"substance_type": "protein",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVITREAL",
"spl_meta": {
"5d1dc1fa-a2d3-46ed-9e9a-c1a036590d3d": {
"match": "brand_token",
"title": "BEOVU (BROLUCIZUMAB) INJECTION, SOLUTION [NOVARTIS PHARMACEUTICALS CORPORATION]",
"spl_version": "16",
"published_date": "2025-11-17"
}
},
"productid": "0078-0827_8b8e71f4-7d7e-40b5-a942-89ac3b6c0c6c",
"productndc": "0078-0827",
"dosage_form": "INJECTION, SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "BROLUCIZUMAB",
"proprietary_name": "BEOVU",
"active_ingred_unit": "mg/.05mL",
"application_number": "BLA761125",
"marketing_category": "BLA",
"nonproprietary_name": "brolucizumab",
"start_marketing_date": "20191007",
"active_numerator_strength": "6"
}Related drugs
Other records sharing ATC code S01LA06.
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