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United States · US · US:50242-082_71a6df7b-906b-4de9-ad4f-200285958cdc
LUCENTIS
UNIISPLATC S01LA04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerGenentech, Inc.
CountryUS (United States)
ATC codeS01LA04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1150242082031 SYRINGE, GLASS in 1 CARTON (50242-082-03) / .05 mL in 1 SYRINGE, GLASS
- ndc1150242082881 SYRINGE, GLASS in 1 CARTON (50242-082-88) / .05 mL in 1 SYRINGE, GLASS
Annotations
UNII (FDA Substance ID)
ZL1R02VT79
RANIBIZUMAB
RxCUI 595060
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "ZL1R02VT79",
"rxcui": "595060",
"inchikey": null,
"display_name": "RANIBIZUMAB",
"substance_type": "protein",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVITREAL",
"spl_meta": {
"de4e66cc-ca05-4dc9-8262-e00e9b41c36d": {
"match": "brand_token",
"title": "LUCENTIS (RANIBIZUMAB) INJECTION, SOLUTION [GENENTECH, INC.]",
"spl_version": "27",
"published_date": "2025-11-26"
}
},
"productid": "50242-082_71a6df7b-906b-4de9-ad4f-200285958cdc",
"productndc": "50242-082",
"dosage_form": "INJECTION, SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "RANIBIZUMAB",
"proprietary_name": "LUCENTIS",
"active_ingred_unit": "mg/mL",
"application_number": "BLA125156",
"marketing_category": "BLA",
"nonproprietary_name": "RANIBIZUMAB",
"start_marketing_date": "20120810",
"active_numerator_strength": "6"
}Related drugs
Other records sharing ATC code S01LA04.
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