Home NDC 85166-001 Lumvoa
Product NDC 85166-001
11-digit product format 851660001
Labeler code 85166
Product ID 85166-001_b2e929f4-7a8c-4289-98aa-4f042e645c3a
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name veligrotug
Dosage form INJECTION
Route INTRAVENOUS
Labeler Viridian Therapeutics, Inc.
Application BLA761530
Marketing category BLA
Marketing start 2026-06-26
Substance VELIGROTUG
Active strength 50 mg/mL
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Lumvoa
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength VELIGROTUG 50 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination Z9U2SS9ZC8 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2746009 Internal RxNorm lookup 2746016 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Purple Book Biologic Products# BLA, Proprietary name, Proper name table BLA Proprietary name Proper name License type Status Latest source 761530 Lumvoa veligrotug-vvze 351(a) Rx 2026-08-01
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Status 85166-001-01 85166000101 1 VIAL, SINGLE-DOSE in 1 CARTON (85166-001-01) / 10 mL in 1 VIAL, SINGLE-DOSE 2026-06-26 0 Current