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United States · US · US:0002-7722_e1015232-2dfd-4b5d-b1d0-e0302e49c55a
Omvoh
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerEli Lilly and Company
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1100027722111 KIT in 1 CARTON (0002-7722-11) * 1 mL in 1 SYRINGE (0002-8870-01) * 2 mL in 1 SYRINGE (0002-1442-01)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "SUBCUTANEOUS; SUBCUTANEOUS",
"spl_meta": {
"472cbe04-263e-433d-9a0f-58c1b50b715a": {
"match": "brand_token",
"title": "OMVOH (MIRIKIZUMAB-MRKZ) INJECTION, SOLUTION OMVOH (MIRIKIZUMAB-MRKZ) KIT [ELI LILLY AND COMPANY]",
"spl_version": "18",
"published_date": "2025-12-19"
}
},
"productid": "0002-7722_e1015232-2dfd-4b5d-b1d0-e0302e49c55a",
"productndc": "0002-7722",
"dosage_form": "KIT",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": null,
"proprietary_name": "Omvoh",
"active_ingred_unit": null,
"application_number": "BLA761279",
"marketing_category": "BLA",
"nonproprietary_name": "mirikizumab-mrkz",
"start_marketing_date": "20250115",
"active_numerator_strength": null
}Access this data programmatically
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