# Omvoh

NDC: 0002-7722
Generic name: mirikizumab-mrkz
Labeler / Manufacturer: Eli Lilly and Company
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: KIT
Routes: SUBCUTANEOUS
Marketing started: 20250115

FDA application: BLA761279

## Active ingredients

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## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0002-7722"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0002-7722
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=472cbe04-263e-433d-9a0f-58c1b50b715a