# Lumvoa

NDC: 85166-001
Generic name: veligrotug
Labeler / Manufacturer: Viridian Therapeutics, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20260626

FDA application: BLA761530

## Active ingredients

- VELIGROTUG: 50 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"85166-001"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=85166-001
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=11bc286a-5411-45af-af3f-69ad38efb610